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Feasibility of a group-based laughter yoga intervention as an adjunctive treatment for residual symptoms of depression, anxiety and stress in people with depression.

Journal of affective disorders
April 1, 2019
Daniel Bressington et al. (8 authors)
Journal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to investigate the feasibility and potential efficacy of Laughter Yoga (LY) for improving residual mood, anxiety, and stress symptoms in adults diagnosed with depression.

Results Summary

The LY group showed statistically greater decreases in depression and improvements in mental health-related quality of life compared to the control group immediately post-intervention. Participants reported high satisfaction with the intervention, though qualitative feedback suggested some aspects required modification.

Population

Working-aged adults with a clinical diagnosis of depression.

Effective Dosage

Eight sessions over four weeks.

Duration

Four weeks (with follow-up at three months).

Interactions

None mentioned

Extracted Claims (5)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Laughter Yoga (LY)
decrease
depressive symptoms
-
-
reduces
#1
Laughter Yoga (LY)
decrease
depression
adults diagnosed with depression
-
had statistically greater decreases in
#2
Laughter Yoga (LY)
increase
mental health related quality of life
adults diagnosed with depression
-
improvements in
#3
Laughter Yoga (LY)
increase
depression
-
-
may be effective to improve
#4
Laughter Yoga (LY)
increase
mental health related quality of life
-
-
may be effective to improve
#5
Abstract

BACKGROUND: Laughter Yoga (LY) is a group-based intervention involving simulated laughter, gentle stretching, rhythmic breathing and meditation. There is some limited evidence that LY reduces depressive symptoms over the short term. However, the quality of previous LY studies is poor and none involved working-aged people with a clinical diagnosis of depression. Therefore, this study aimed to investigate the feasibility and potential efficacy of LY for improving residual mood, anxiety and stress symptoms in adults diagnosed with depression. METHODS: Fifty participants were randomised to the group LY intervention (n = 23) consisting of eight sessions over four weeks, or treatment-as-usual (n = 27). Participants completed the Depression Anxiety Stress Scale and the Short Form 12 item Health Survey at baseline (T0), post-intervention (T1) and at 3 months follow-up (T2). LY participants also completed a Client Satisfaction Questionnaire (CSQ8) at T1 and eleven participated in individual qualitative interviews at T2. RESULTS: The LY group had statistically greater decreases in depression and improvements in mental health related quality of life compared to the control group from T0 to T1. The CSQ8 scores indicated a favourable level of satisfaction with the LY intervention. The qualitative interviews highlighted aspects of the intervention that were effective and those requiring modification. LIMITATIONS: Limitations include the small sample size and treatment-as-usual control group. CONCLUSIONS: A full scale RCT of LY could be feasible if some modifications were made to the protocol/intervention. The intervention may be effective to improve depression and mental health related quality of life immediately post intervention.

Medical Subject Headings (MeSH)
AdolescentAdultAffectAnxietyAnxiety DisordersDepressive DisorderFeasibility StudiesFemaleHumansLaughter TherapyMaleMeditationMental HealthMiddle AgedPatient SatisfactionProspective StudiesQuality of LifeStress, PsychologicalSurveys and QuestionnairesYogaYoung Adult
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality70/10
Citation Metrics
Total Citations26
Citations/Year4.3
Relative Citation Ratio2.26
NIH Percentile78.1%
Research Impact Scores
APT Score0.75
Weight Score2.14
Normalized Score0.64
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