Effect of laughter exercise versus 0.1% sodium hyaluronic acid on ocular surface discomfort in dry eye disease: non-inferiority randomised controlled trial
BMJ 2024; 386 doi: https://doi.org/10.1136/bmj-2024-080474 (Published 11 September 2024) Cite this as: BMJ 2024;386:e080474
- Jing Li, ophthalmologist1,
- Yinglin Liao, doctoral student1,
- Shi-Yao Zhang, doctoral student1,
- Ling Jin, statistician1,
- Nathan Congdon, professor1 2 3,
- Zixin Fan, ophthalmologist1,
- Yangfa Zeng, professor1,
- Yingfeng Zheng, professor1,
- Zuguo Liu
, professor4 5, - Yizhi Liu, professor1,
- Lingyi Liang, professor1
- 1State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou, Guangdong, China
- 2Centre for Public Health, Queen’s University Belfast, Belfast, Belfast, UK
- 3Orbis International, New York, NY, USA
- 4Xiamen University affiliated with Xiamen Eye Center, Fujian Provincial Key Laboratory of Ophthalmology and Visual Science, Fujian Engineering and Research Center of Eye Regenerative Medicine, Eye Institute of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, China
- 5Department of Ophthalmology, The First Affiliated Hospital of University of South China, Hengyang, Hunan, China
- Correspondence to: L Liang lianglingyi{at}gzzoc.com
- Accepted 1 August 2024
Abstract
Objective To assess efficacy and safety of laughter exercise in patients with symptomatic dry eye disease.
Design Non-inferiority randomised controlled trial.
Setting Recruitment was from clinics and community and the trial took place at Zhongshan Ophthalmic Center, Sun Yat-sen University, the largest ophthalmic centre in China, between 18 June 2020 to 8 January 2021.
Participants People with symptomatic dry eye disease aged 18-45 years with ocular surface disease index scores ranging from 18 to 80 and tear film break-up time of eight seconds or less.
Interventions Participants were randomised 1:1 to receive laughter exercise or artificial tears (0.1% sodium hyaluronic acid eyedrop, control group) four times daily for eight weeks. The laughter exercise group viewed an instructional video and participants were requested to vocalise the phrases “Hee hee hee, hah hah hah, cheese cheese cheese, cheek cheek cheek, hah hah hah hah hah hah” 30 times per five minute session. Investigators assessing study outcomes were masked to group assignment but participants were unmasked for practical reasons.
Main outcome measures The primary outcome was the mean change in the ocular surface disease index (0-100, higher scores indicating worse ocular surface discomfort) from baseline to eight weeks in the per protocol population. The non-inferiority margin was 6 points of this index score. Main secondary outcomes included the proportion of patients with a decrease from baseline in ocular surface disease index score of at least 10 points and changes in dry eye disease signs, for example, non-invasive tear break up time at eight weeks.
Results 299 participants (mean age 28.9 years; 74% female) were randomly assigned to receive laughter exercise (n=149) or 0.1% sodium hyaluronic acid (n=150). 283 (95%) completed the trial. The mean change in ocular surface disease index score at eight weeks was −10.5 points (95% confidence interval (CI) −13.1 to −7.82) in the laughter exercise group and −8.83 (−11.7 to −6.02) in the control group. The upper boundary of the CI for difference in change between groups was lower than the non-inferiority margin (mean difference −1.45 points (95% CI −5.08 to 2.19); P=0.43), supporting non-inferiority. Among secondary outcomes, the laughter exercise was better in improving non-invasive tear break up time (mean difference 2.30 seconds (95% CI 1.30 to 3.30), P<0.001); other secondary outcomes showed no significant difference. No adverse events were noted in either study group.
Conclusions The laughter exercise was non-inferior to 0.1% sodium hyaluronic acid in relieving subjective symptoms in patients with dry eye disease with limited corneal staining over eight weeks intervention.
Trial registration ClinicalTrials.gov NCT04421300.
Introduction
Dry eye disease is a widespread, complex ocular surface disease characterised by chronic subjective ocular discomfort, tear film instability, and visual disturbance.123 With the population ageing, video display terminal use increasing, and air pollution, the global prevalence of dry eye disease has risen sharply, affecting approximately 360 million individuals.4 Use of artificial tears is the mainstay treatment for dry eye disease. Although not fatal, dry eye disease substantially reduces life quality and is a substantial economic burden, particularly among long term users of artificial tears.5 The global artificial tears market had a revenue share of USD 2.74 billion in 2022 (£2.12 billion, €2.53 billion), expected to advance to USD 4.40 billion by 2031.6 Additionally, the societal costs such as lost work productivity and the psychological and physical impacts of dry eye disease, are estimated at $55 billion in the US.7
Studies across multiple geographies and populations have reported the correlation between dry eye disease and mental health, particularly in negative emotions such as depression and anxiety.89101112 In people with depression or anxiety, the link is stronger for dry eye disease symptoms as compared with patient signs.810131415 These results suggest that the connection between dry eye disease symptoms and depression or anxiety does not appear to be driven by dry eye disease signs.11
In recognition of the importance of positive psychology, the World Health Organization considers happiness as a crucial component of overall well being.16 Individuals with higher levels of subjective happiness report fewer symptoms of dry eye disease,1718 however, the impact of positive emotions on dry eye disease remains uncertain.
In accordance with the well known saying “laughter is the best medicine”, laughter therapy was first reported by Cousins in 1979, primarily involving mimicking mouth shapes while enunciating “hahahoho.”19 Research findings suggested laughter might be therapeutic to reduce disease symptoms.20 At present, laughter therapy comprises various interventions designed to provoke laughter, smiling, and pleasant feelings such as laughter exercises, clowns, comedy movies, games, and puzzles.21 Abundant evidence suggests that laughter therapy alleviates depression, anxiety, stress, and chronic pain, while strengthening immune function222324; and therefore, it has been recognised as a complementary and adjunctive approach for chronic conditions like mental health disorders, cancer, diabetes, among others.252627282930 Whether laughter therapy has a beneficial effect on dry eye disease, a chronic condition closely related to mental health and lifestyle,31 remains unknown. In our pilot studies before the randomised controlled trial, we observed that laughter could immediately improve tear film stability and lipid layer thickness (protocol, pages 12-13 in supplementary file, data unpublished). Additionally, in a small scale study, we found that laughter exercise could alleviate symptoms of dry eye disease (protocol, pages 15-16 in supplementary file, data unpublished).
In this study, we conducted a randomised trial to compare the effectiveness of laughter exercise versus artificial tears in treating symptomatic dry eye disease. The hypothesis was that non-inferiority would be established by observing a between-group difference in the ocular surface disease index score of ≤6 points in eight weeks between the laughter exercise group and the controls, who were using the mainstay treatment of artificial tears. We chose a non-inferiority trial design because laughter exercise is a safe, environmentally friendly, and low cost intervention.
Methods
Study design
In this two arm, non-inferiority randomised controlled trial, the setting was at a single tertiary referral centre, Zhongshan Ophthalmic Center, Sun Yat-sen University, which is the largest ophthalmic centre in southern China. All procedures adhered to the protocol approved by the ethics committee of Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China (2020KYPJ010). Written informed consent was obtained from all participants. The trial protocol and statistical analysis plan are available in the supplementary files.
Participants
Participants with symptomatic dry eye disease were recruited from cornea and ocular surface disease clinics and locations surrounding the hospital using community advertisements, flyers, and via social media. All participants passed a screening examination 14 days before inclusion. Screening included a medical history and subjective assessment of dry eye disease symptoms using the ocular surface disease index. The international dry eye workshop in 2007 and 2017, emphasised that dry eye disease is a symptomatic disease, and symptom questionnaires are among the most reliable diagnostic tests available.3233 The ocular surface disease index is a 12-item index measuring ocular discomfort, with scores ranging from 0 to 100, with 0 indicating the least discomfort and 100 the greatest.
Participants were required to fulfil the diagnostic criteria of the global consensus tear film and ocular surface association dry eye workshop II for dry eye disease.32 Participants were also required to have the ocular surface disease index score of 18 to 80 at both the screening and the eligibility confirmation visits approximately two weeks later, and a fluorescein tear break-up time (time from a blink to the appearance of the first gap in the tear film, with shorter times indicating worse tear film stability) of eight seconds or less at eligibility confirmation visit. Exclusion criteria included a score from the National Eye Institute’s corneal fluorescein staining examination of more than 5 (range 0-15, with higher scores indicating more severe corneal epithelial defects); use of any dry eye disease treatment in the 14 days before enrolment; contact lens usage within 14 days before screening visit; inability to guarantee no contact lens wear for three months after trial participation; any eye surgery or history of ocular trauma within the past 12 months; any history of eye infection or allergy within the past three months; severe ocular surface scarring or conditions that could compromise the integrity of the ocular surface, such as Steven-Johnson syndrome; any previous diagnosis of glaucoma or treatment with glaucoma medications; and the presence of neurological, psychiatric or, sleep disorders. We did not enrol anyone with cognitive or comprehension deficits who could not co-operate with the eye examination, questionnaire completion, or use of the face recognition application study application laughing face, or who had major life changes, such as planning to move to another city within the next three months, or were fearful of the bright light from eye examination equipment for this study. A complete list of the inclusion and exclusion criteria is provided in the protocol (pages 20-22).
All participants were shown the protocol and signed patient consent forms.
Randomisation and masking
Stratified block randomisation was applied with a block size of four. Participants were stratified based on their baseline ocular surface disease index scores (mild ≤18 to <23, moderate ≤23 to <33 and severe ≤33 to <80). Within each stratum, patients were randomly assigned in a 1:1 ratio to receive either laughter exercise or 0.1% sodium hyaluronic acid for eight weeks. The random sequence was generated by an independent statistician who was not involved in project implementation, using an online generator. The randomisation assignment was kept undisclosed to the trained investigators responsible for screening and outcome assessment. Participants were unmasked to group assignment but were masked to trial hypotheses.
Intervention
Drawing from previously established methods of laughter therapy, we adapted and developed the laughter exercise (supplementary video) to optimally engage the ocular muscles of participants. Participants were instructed to perform the laughter exercise four times daily for eight weeks. At the baseline visit, an instructional video showed the execution of the exercise. Specifically, laughter exercise required participants to vocalise and repeat the phrases as “Hee hee hee, hah hah hah, cheese cheese cheese, cheek cheek cheek, hah hah hah hah hah hah” 30 rounds each time, lasting for at least five minutes (video 1, video 2). To standardise the laughter exercise and enhance facial movements throughout the session, participants used a face recognition application on their mobile devices that had been designed by authors, named laughing face, at the start of each session (supplementary figure 1). The app was developed in collaboration with South China University of Technology and Xinhuixing Information Technology, Inc (Guangzhou, China). Following the eight week intervention, participants ceased the exercise and underwent follow-up at the week 10 and 12.
Instructions given to the laughter exercise group translated into English
Instructions given to the laughter exercise group in Mandarin Chinese video
Participants in the control group applied artificial tears, 0.1% sodium hyaluronic acid eyedrops, to both eyes four times daily for eight weeks, tracking their usage frequency via the laughing face app. After the eight week treatment, they were instructed to discontinue the eye drops and returned for follow-up appointments at weeks 10 and 12.
The participants were followed up on weekends for their convenience. Participants in both groups were encouraged to continue their routine activities during the 12 week study period. Adherence was supported through an oral and written commitment from all participants at the baseline evaluation. For daily record keeping, participants in both study groups used the laughing face app, for which they were provided with individual access codes. The app provided daily text reminders to complete the study interventions. Those in the laughter exercise group were requested to practice with the app before each laughter session and upload their exercise videos at least once a day. All participants used the app to log their exercise sessions or eye drops use. If a participant missed an exercise session or eye drop application, they were prompted by the app to make up for the missed session. Throughout the eight week period, we tracked the number of missed exercise sessions and eye drops applications as a measure of compliance.
Outcomes
The primary outcome was the mean change in the ocular surface disease index score from baseline to eight weeks. Prespecified secondary outcomes included: the proportion of patients with a decrease from baseline in the ocular surface disease index score of 10 points or more (ie, the minimal clinically meaningful cut-off34), changes in signs of dry eye disease as assessed by non-invasive tear break up time, corneal fluorescein staining score, tear meniscus height, changes in the scores on the physical and mental health subscales of the 36-item short form health survey35 (scores range from 0 to 100, with higher scores indicating better health-related quality of life), changes in the scores of self-rating anxiety scale36 and self-rating depression scale37 (scores range from 0 to 100, with higher indicating severe self-report anxiety or depression), changes in the scores of Pittsburgh sleep quality index38 (scores range from 0 to 21, with higher scores indicating worse sleep quality), changes in the scores of subjective happiness scale39 (scores range from 1 to 7, with higher scores indicating a higher level of happiness). Because of the inconsistent correlation between reported symptoms and clinical signs, we chose non-invasive tear break up time as the main secondary outcome. The details and examination procedures of exploratory outcomes including function and structure of meibomian gland were described in the trial protocol (supplementary file).
Participants were scheduled to return on day seven for assessments, after that at two weeks, four weeks, six weeks, and eight weeks (the last day of treatment and the time of assessment for the main study outcome), and again at 10 and 12 weeks. We monitored adverse events throughout the treatment period using a standard adverse event case report form at each visit.
Statistical analysis
Sample size estimation
The trial was designed to enrol 296 participants (n=148 in each group), reaching 90% statistical power to detect non-inferiority at a one-sided α=0.025 based on the primary outcome using a one sided, two sample t-test. We selected a non-inferiority margin of 6 points, which is 50% of the minimum meaningful clinical difference on the ocular surface disease index,32 with the common standard deviation of 15. The true difference between means was assumed to be 0.00, and loss to follow up less than 10%. Non-inferiority would be established by a one sided test of the 97.5% confidence interval (CI) of the difference in trial arms that was less than the non-inferiority margin. This margin would be equivalent to testing whether a two sided 95% CI around the treatment difference falls within the non-inferiority margin. The sample size was calculated using PASS 16.0.
Data analyses
We developed a statistical analysis plan before final analysis (supplementary file). No interim analysis was undertaken. The trial was registered at ClinicalTrials.gov (NCT04421300) on 5 June 2020. The first participant was enrolled on 3 July 2020. The participants’ baseline characteristics were described as mean (standard deviation) or median (interquartile range) for continuous variables, and frequency (percentage) for categorical variables. The normality of continuous data was checked using the Shapiro-Wilk test and histograms.
Both per protocol and the intention-to-treat analyses were used in calculating the adjusted difference and 95% CI for the primary outcome, and intention to treat was used in calculating unadjusted difference and 95% CI for secondary outcomes. In intention-to-treat analysis, all participants undergoing randomisation were included, and all missing data were imputed using multiple imputations, creating 20 copies of the data. Results were obtained by averaging these 20 datasets using Rubin’s rules.40
Line and box plots were drawn to show the outcome’s change across time. Generalised estimated equation model with adjustment for intra-eye correlation was applied for the comparisons of clinical outcomes, which were measured in both right and left eyes. The difference between groups was tested using the two sample t-test for primary and psychological outcomes, and generalised estimated equation model for all clinical outcomes. Pre-post changes were tested with the paired t-test for primary and psychological outcomes and generalised estimated equation models for all clinical outcomes.
Data were cleaned using Stata16.0 and all statistical analyses were performed using SAS 9.4. A two sided P value less than 0.05 was considered statistically significant. For secondary outcomes, P for between group difference was adjusted by the Benjamini-Hochberg method with a false discovery rate of 0.05 for multiple comparisons. P values for exploratory outcomes were not calculated.
Patients and public involvement
Although patients or the public were not involved in the design, or conduct, or reporting, or dissemination plans of our research, they did participate in the preliminary study. Participants provided suggestions for implementing our laughter exercise, including the number of repetitions per section, the frequency of daily interventions, and how to improve communication between the research team and patients. Moreover, the results were communicated to patients who expressed an interest after the completion of the study.
Results
Between 18 June 2020 and 8 January 2021, 1335 volunteers were screened for eligibility (fig 1). Of these, 665 (50%) volunteers met none of the exclusion criteria and were scheduled to attend an eligibility confirmation visit two weeks later. Of the 613 (92%) people presenting for the examination, 299 (49%) were eligible for inclusion in the trial and were randomly assigned (1:1) to the laughter exercise group or the 0.1% sodium hyaluronic acid (control) group. The intention-to-treat population, therefore, included 149 participants in the intervention group and 150 participants in the control group. Table 1 shows the baseline data for the 299 participants who were randomly allocated a group. Participants had a mean age of 28.9 (6.30) years, 74% (78/299) were women, 95% (283/299) have more than 12 years of education. The high proportion of female participants is consistent with the general population in that women are more likely to have dry eye disease than men.54142 Baseline characteristics were well balanced between the two groups. In the laughter exercise group, 92% (137/149) of participants completed the scheduled follow-up visits at 12 weeks, and that in the control group was 98% (146/150). The median of the cumulative compliance during the eight week treatment was 85% (interquartile range 65-96%) for the laughter exercise group and 81% (68-90%) for the control group.
Flow of participants through trial. HA=hyaluronic acid; OSDI=ocular surface disease index
Baseline characteristics of study participants
The primary outcome of mean change in the score of the ocular surface disease index from baseline to eight weeks was −10.5 points (95% CI −13.1 to −7.82) in the laughter exercise group and −8.83 (−11.7 to −6.02) in the control group. The decrease in the ocular surface disease index scores was statistically significant in both groups at eight weeks compared with baseline (both P<0.001). The upper boundary of the confidence interval for the mean between group difference in change between laughter exercise and control was lower than the non-inferiority margin of 6 points (−1.45 points (95% CI −5.08 to 2.19); P=0.43), suggesting that the laughter exercise is not inferior to 0.1% sodium hyaluronic acid eyedrops (fig 2). The intention-to-treat analysis showed similar results (difference between the two groups was −1.32 points, 95% CI −4.90 to 2.26; P=0.47)(table 2). Both treatments were stopped at eight weeks at the trial end, with further evaluations made at 12 week. The laughter exercise group had a persistent and significantly greater decrease in the ocular surface disease index score than did the control group at 12 weeks (table 2, fig 2, supplementary figure 2): the mean between group difference was −4.08 points ((95% CI −7.62 to −0.55); P=0.024).
The non-inferiority comparison between laughter exercise group and 0.1% sodium hyaluronic acid group. The upper bound of the 95% confidence interval (CI) −5.08 to 2.19 at eight weeks was less than the non-inferiority margin which had been prespecified as 6, indicating that laughter exercise was not inferior to 0.1% sodium hyaluronic acid at the primary end point, and tended to be converted to superiority at 12 weeks with the whole 95% CI below the zero line (−7.62 to −0.55). OSDI=ocular surface disease index
Adjusted effect of laughter exercise on primary outcome of OSDI score at eight weeks
The secondary outcome of the proportion of participants whose ocular surface disease index score decreased by at least 10 points at eight weeks was 49.3 percentage points (95% CI 41.0 to 57.5) in the laughter exercise group versus 47.3 (39.3 to 55.3) in the 0.1% sodium hyaluronic acid group (mean difference 1.96 (95% CI −9.53 to 13.5); P≥0.05)(table 3). After eight weeks of treatments, the laughter exercise group had a more significant improvement in non-invasive tear break up time than did the control group, with a mean between group difference was 2.30 seconds ((95% CI 1.30 to 3.30); P<0.001) in the change from baseline to eight weeks (supplementary figure 3A). Changes in other secondary outcome measures (supplementary figure 3B-F) were not significant between the groups (all P≥0.05). As for the subjective scale scores, improvements were noted in the self-rating anxiety scale and self-rating depression scale score between baseline and eight weeks in both groups (all P<0.01 for the change in each group, but no significant change between groups), but not in the subjective happiness scale and Pittsburgh sleep quality index scores (table 3). Additionally, the laughter exercise group showed a significant improvement in the mental health subscale of the 36-item short form health survey after eight weeks (table 3).
Intention to treat analysis: unadjusted effect of laughter exercise on clinical signs of dry eye disease at eight weeks
For the exploratory outcomes (table 3), the laughter exercise group showed amelioration in fluorescein tear break-up time by 1.82 seconds (95% CI 1.60 to 2.03), better than that in 0.1% sodium hyaluronic acid group (mean difference 1.50 seconds (95% CI 1.23 to 1.76)). Moreover, the function of the meibomian gland was improved only in the laughter exercise group, with the meibomian gland secretory capacity improved by −0.24 (95% CI −0.33 to −0.14), and meibomian gland secretion property score improved by −3.78 (−4.45 to −3.12). The above clinical signs for monocular results were consistent with those for binoculars (supplementary table 1).
No adverse events were reported in either study group.
Discussion
Principal findings
Our results showed that laughter exercise was non-inferior to 0.1% sodium hyaluronic acid in alleviating dry eye disease symptoms. Additionally, we found that laughter exercise appeared to improve tear film stability and the meibomian gland function. We observed high cumulative compliance rates in the laughter exercise group.
Dry eye disease imposes an economic burden on both society and individuals because of healthcare use, such as repeated medical visits and long term eyedrops. Artificial tears are the mainstay of treatment for dry eye disease, and 0.1% sodium hyaluronic acid, one of the most widely used artificial tears, has a proven therapeutic effect in alleviating subjective ocular discomfort, and stabilising tear film in patients with dry eye disease. In terms of alleviating symptoms, laughter exercise was non-inferior to 0.1% sodium hyaluronic acid in the per protocol and intention-to-treat analyses in our study. The primary outcome was ocular surface disease index score, a well validated and widely used tool for outcome assessment in clinical trials of dry eye disease.3234 Moreover, laughter exercise significantly improved tear film stability and meibomian gland function. These benefits persisted for at least four weeks after discontinuation of the exercise, and such lasting efficacy was not noted in 0.1% sodium hyaluronic acid group.
Possible mechanisms
The biological mechanisms of laughter exercise on dry eye disease are unclear. Lacrimal gland, which secretes aqueous tears, and meibomian gland, which secretes lipid, are both innervated dominantly by parasympathetic nerves.43 In the motor system, vocalisations in laughter involve the motoneuronal cell groups innervating the soft palate, pharynx, and larynx as well as the diaphragm, intercostal, abdominal, and pelvic floor muscles.44 The contraction of respiratory muscles in laughter, especially abdominal breathing,45 stimulates the autonomic nervous system including the activation of sympathetic and parasympathetic nervous system.4647 Consequently, laughter exercise stimulates tear secretion via autonomic nervous system activation.48
Notably, the contraction of orbicularis muscle (sphincter muscles of the eyelids) during laughter exercise is another plausible explanation. According to our results, patients in the laughter exercise group had greater improvements in the secretory capacity of the meibomian gland and properties of its secretion, when compared with 0.1% sodium hyaluronic acid. During the laughter exercise, patients were instructed to perform the vocalisations aloud and exaggerate their facial expressions, thus contracting the orbicularis oculi muscle, which function as the sphincter muscles of the eyelids, and are anatomically adjacent to the meibomian glands.49 The contraction of the Riolan muscle, a distinct subdivision of striated orbicularis muscle, compresses the ductules of the meibomian gland, resulting in the extrusion of lipids onto the ocular surface.50 Lipid tears are essential in maintaining tear film stability by delaying tear evapouration.51
Research has indicated that positive emotions in non-human animals can induce tear secretion through the release of oxytocin,52 which could be triggered by laughter.53 In our study, we hypothesised that positive emotions may also prompt tear secretion through deep breathing, relaxation, and laughter during the laughter exercise. The biological mechanisms underlying this effect is warranted further study.
Dry eye disease is not only a topical disease but also a systemic disease including brain and lifestyle.1154 Evidence indicates that lifestyle factors such as mental health can induce or modulate the severity of symptoms and signs of dry eye disease.115556 Symptoms of dry eye disease are closely associated with anxiety and depression.1157 Individuals with higher levels of subjective happiness have reported fewer symptoms of dry eye disease.1718 Laughter positively affects cognitive behaviour to improve and establish healthy physical, psychological, and social relationships, and thereby quality of life.585960 A study published in 2022 indicated that a facial mimicry laughter could both amplify and initiate feelings of happiness, regardless of the presence or absence of emotional stimuli.61 We modified our laughter exercise by facial mimicry and voluntary facial action tasks, which might have a similar positive effect to laughter.61 Evidence suggests that laughter therapy is a tool in lifestyle medicine that can improve sleep quality, and physical and psychological functions (eg, body weight, subjective stress, subjective well being),62 and promote energy expenditure.636465 We also observed the improved mental health score in laughter exercise group. More frequent daily laughter is associated with a lower prevalence of lifestyle related diseases, such as hypertension, diabetes mellitus, and heart disease.66 Thus, laughter exercise might alleviate dry eye disease indirectly by creating a persisting positive effect on lifestyle. This effect might also explain the continued improvement in ocular surface disease index observed between eight and 12 weeks, following the termination of the trial.
Strengths and limitations of this study
Strengths of this trial include the randomised controlled design, careful compliance monitoring and support, high rates of both compliance and follow-up, and good effort to standardise the laughter exercise intervention with the use of videos.
However, our study had limitations. A double blinded study design was not practical because this would necessitate a sham laughter exercise for which no approach has been validated. To minimise possible placebo effects, participants were informed that the study aimed to compare the effects of two different interventions without alluding to the possible effects of laughter exercise. Additionally, laughter exercise has a greater time investment when compared with the use of eyedrops, albeit minimal.
Future directions
Future research should assess the most effective frequency and duration of laughter exercise. The biological mechanisms warrant further testing by experimental studies. Furthermore, research into laughter exercise for other ocular conditions compared with other artificial tears, with or without lipids, and higher concentrations of sodium hyaluronic acid, would provide a more comprehensive understanding of therapeutic potential. Moreover, the association between dry eye disease and lifestyle disorders is complicated, and a comprehensive approach should be investigated in the future.
Conclusions
The findings of this randomised controlled trial suggest that laughter exercise, four times a day, was non-inferior to 0.1% sodium hyaluronic acid, four times a day, in improving dry eye disease symptoms and clinical signs. As a safe, environmentally friendly, and low cost intervention, laughter exercise could serve as a first-line, home based treatment for people with symptomatic dry eye disease and limited corneal staining.
What is already known on this topic
Dry eye disease is a chronic condition worldwide linked with psychological stress and poses an economic burden of long term use of artificial tears
0.1% sodium hyaluronic acid, a widely used artificial tear, has a proven therapeutic effect for ocular discomfort, and stabilising tear film in patients with dry eye disease
Laughter therapy is recognised as a beneficial complementary and adjunctive treatment for various chronic conditions, including mental health disorders, cancer, and diabetes
What this study adds
Laughter exercise was non-inferior to artificial tears (0.1% sodium hyaluronic acid) in improving dry eye disease symptoms and clinical signs
Laughter exercise is a safe, environmentally friendly, and low cost intervention for patients with symptomatic dry eye disease and limited corneal staining
Ethics statements
Ethical approval
Ethical approval was obtained from the Ethics Committee of Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China (2020KYPJ010). Written informed consent was obtained from all participants.
Data availability statement
All data requests should be submitted to lianglingyi@gzzoc.com for consideration. Access to anonymised data may be granted after review.
Footnotes
Contributors: JL, YLia, and S-YZ contributed equally to the study and are joint first authors. LL, ZL, and YLiu conceived and designed the study. LL, JL, YLia, S-YZ, LJ, ZF, ZL, YLiu conducted the study, including acquisition, analysis, or interpretation of data. LJ and NC were responsible for statistical analysis. JL, LL, LJ, and NC drafted the manuscript. JL and LL obtained funding. LL, JL, LJ, NC, YZe, YZh, ZL, and YLiu were responsible for administrative, technical, or material support. LL, YZe, YZh, YLiu, and ZL were responsible for study supervision. All authors critically revised the manuscript. All authors gave final approval of the manuscript. LL, YLiu, and ZL contributed equally to this work and are the joint corresponding authors. LL is the guarantor. The corresponding author attests that all listed authors meet authorship criteria and that no others meeting the criteria have been omitted.
Funding: The study was funded by the National Natural Science Foundation of China (grant number 82070922, 82201142); and the High-level Hospital Construction Project (grant number 303020101). The funders had no role in considering the study design or in the collection, analysis, interpretation of data, writing of the report, or decision to submit the article for publication.
Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/disclosure-of-interest/ and declare: support from the National Natural Science Foundation of China (82070922, 82201142) and the High-level Hospital Construction Project (303020101) for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.
Patient consent: Patient consent obtained.
Transparency: The manuscript’s guarantor (LL) affirms that the manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as originally planned have been explained.
Dissemination to participants and related patient and public communities: A link to the publication will be sent to the research participants. The main findings of this trial will be disseminated to clinicians, patients and to the public via press releases, social media, and educational and training materials; presented to the scientific community at academic conferences; and shared with clinicians caring for patients with dry eye disease.
Provenance and peer review: Not commissioned; externally peer reviewed.
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