NCT07524231

Brief Summary

This randomized controlled study aims to evaluate the effects of laughter yoga on pain intensity, fatigue, and beta-endorphin levels in patients with Multiple Sclerosis. Laughter yoga, a complementary therapy combining breathing exercises and laughter techniques, may help improve symptom management and psychological well-being in individuals with MS.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable multiple-sclerosis

Timeline
4mo left

Started Mar 2026

Shorter than P25 for not_applicable multiple-sclerosis

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress25%
Mar 2026Aug 2026

Study Start

First participant enrolled

March 10, 2026

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

March 11, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 10, 2026

Last Updated

April 13, 2026

Status Verified

March 1, 2026

Enrollment Period

4 months

First QC Date

March 11, 2026

Last Update Submit

April 6, 2026

Conditions

Keywords

Multiple SclerosispainLaughter Yoga,fatigue

Outcome Measures

Primary Outcomes (1)

  • Change in pain intensity measured by Visual Analog Scale (VAS) at [time point]

    Pain intensity will be assessed using the Visual Analog Scale (VAS), a 10 cm scale ranging from 0 (no pain) to 10 (worst imaginable pain). Participants will indicate their pain level by marking on the scale, and the score will be determined by measuring the distance in centimeters or millimeters.

    Baseline and week 4

Secondary Outcomes (2)

  • Fatigue Level

    1 month

  • Change in plasma beta-endorphin levels measured by ELISA at baseline and week 4

    Baseline and week 4

Study Arms (2)

Experimental Group

EXPERIMENTAL

Patients with Multiple Sclerosis who will receive laughter yoga in addition to routine care.

Behavioral: Laughter Yoga

Control Group

NO INTERVENTION

Patients with Multiple Sclerosis who will receive routine care without laughter yoga.

Interventions

Laughter YogaBEHAVIORAL

A complementary intervention including breathing exercises, stretching, relaxation techniques, and laughter exercises applied to patients with Multiple Sclerosis.

Experimental Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being over 18 years old
  • Being able to communicate adequately
  • Volunteering to participate in the research

You may not qualify if:

  • Unwillingness to participate in the study
  • Having severe cognitive impairment that prevents understanding or participation in the intervention
  • Having a psychiatric disorder that may affect participation in the study
  • Experiencing an acute MS relapse during the study period
  • Having another serious neurological or chronic disease that may affect the study outcomes
  • Regular participation in another complementary therapy program similar to laughter yoga
  • Communication problems that prevent participation in the intervention sessions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gül DURAL

Elâzığ, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Multiple SclerosisPainFatigue

Interventions

Laughter Therapy

Condition Hierarchy (Ancestors)

Demyelinating Autoimmune Diseases, CNSAutoimmune Diseases of the Nervous SystemNervous System DiseasesDemyelinating DiseasesAutoimmune DiseasesImmune System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeutics

Central Study Contacts

Gül DURAL, pHD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

March 11, 2026

First Posted

April 13, 2026

Study Start

March 10, 2026

Primary Completion (Estimated)

July 10, 2026

Study Completion (Estimated)

August 10, 2026

Last Updated

April 13, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations