Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
NCT06705153

The Effect of Laughter Yoga on Symptom Severity, Depression-anxiety-stress, Sleep Quality and Quality of Life in Patients with Irritable Bowel Syndrome

Led by Ataturk University · Updated on 2025-01-03

56

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study will be conducted to evaluate the effect of laughter yoga on symptom severity, depression, anxiety, stress, sleep and quality of life in patients with Irritable Bowel Syndrome (IBS). The following hypotheses will be tested in this study: H1: Laughter yoga reduces symptom severity in patients with IBS. H2: Laughter yoga reduces depression, anxiety and stress in patients with IBS. H3: Laughter yoga improves sleep quality in patients with IBS. H4: Laughter yoga improves quality of life in patients with IBS.

CONDITIONS

Official Title

The Effect of Laughter Yoga on Symptom Severity, Depression-anxiety-stress, Sleep Quality and Quality of Life in Patients with Irritable Bowel Syndrome

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with IBS according to Rome IV criteria
  • Scoring 75 and above on the IBS-SSS score
  • Depression score of 10 or above, anxiety score of 8 or above, and stress score of 15 or above on the DASS-42 scale
  • Age over 18 years
  • Presence of a smartphone or computer capable of video calls for laughter yoga sessions
  • No communication problems
  • Willing to participate in the study and provide consent
Not Eligible

You will not qualify if you...

  • Not practicing laughter yoga
  • Irregular attendance at laughter yoga sessions
  • Changes in treatment regimen during the study
  • Desire to leave the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Erzurum City Hospital

Erzurum, Yakutiye, Turkey (Türkiye), 25070

Actively Recruiting

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Research Team

E

Ebru BALA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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