CClinicalTrials.gg
RecruitingNCT07524231Updated Apr 13, 2026

Evaluation of the Effects of Laughter Yoga

An interventional study of Laughter Yoga in Multiple Sclerosis, sponsored by Firat University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by Firat University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started Mar 2026; still recruiting 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
72
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

Multiple Sclerosis (MS) is a chronic, autoimmune, and demyelinating disease that generally affects the central nervous system in young adults. Multiple Sclerosis is a highly heterogeneous disease, with a wide range of clinical signs and symptoms depending on the area of the central nervous system affected, including motor, sensory, autonomic, and cognitive impairments. Multiple Sclerosis is associated with a broad spectrum of bodily dysfunctions, including motor problems such as muscle weakness, changes in muscle tone, ataxia, abnormal balance, and sensory disturbances. In addition, fatigue, pain, bladder and bowel dysfunction, cognitive and emotional problems, vision problems, speech and swallowing disorders, and sexual dysfunction also affect individuals with MS. Currently, there are 2.5 million MS patients worldwide, and the cost of treatment and care for these patients is quite high.

In addition to medical treatment, traditional and complementary medicine (TCM) methods are used in the treatment of pain and fatigue. Laughter Yoga, a type of yoga that has begun to be applied as a TCM method, was developed by Indian physician Dr. Developed by Madan Kataria in 1995, each laughter yoga session consists of breathing exercises, stretching and relaxation techniques, and laughter exercises. Physiologically, laughter yoga has been reported to increase breathing, relax muscles, stimulate circulation and the immune system, increase endorphin release, thereby increasing pain threshold and tolerance, reduce fatigue, decrease stress hormone levels, strengthen mental function, reduce depression and anxiety, improve sleep quality, and enhance interpersonal relationships and social interaction, thus improving psychological well-being. This research was planned as a randomized controlled experimental study to evaluate the effects of laughter yoga applied to Multiple Sclerosis patients on pain intensity, fatigue, and Beta Endorphin levels.

02

Conditions studied

  • Multiple Sclerosis

Keywords

  • Multiple Sclerosis
  • pain
  • Laughter Yoga,
  • fatigue
03

In context

Multiple Sclerosis

3,460 studies on the registry are indexed under Multiple Sclerosis; 661 are open to participants now.

This study's planned enrollment of 72 is above the median of 50 across 2,342 interventional studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

Firat University is the lead sponsor of 112 studies on the registry; 46 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

    • Being over 18 years old

      • Being able to communicate adequately
      • Volunteering to participate in the research

Exclusion criteria

Exclusion Criteria:

  • 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

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
72 participants (estimated)

Study arms

  • Experimental
    Experimental Group

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

    Behavioral: Laughter Yoga

  • No intervention
    Control Group

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

Interventions

  • BehavioralLaughter Yoga

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

06

What researchers measure

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.

    Time frame: Baseline and week 4

Secondary outcomes

  1. Fatigue Level

    Fatigue severity will be assessed using the Fatigue Severity Scale (FSS), a 9-item questionnaire evaluating fatigue over the past month. Each item is scored on a scale of 0 to 7, with higher scores indicating greater fatigue severity. The Turkish validity and reliability study was conducted by Armutlu et al. in 2007. A change of 0.45 points is considered clinically meaningful.

    Time frame: 1 month

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

    Plasma beta-endorphin levels will be measured using an ELISA method. Blood samples will be collected from participants in the intervention group before and after laughter yoga sessions at week 1 and week 4, and from the control group at week 1 and week 4. Samples will be centrifuged, and serum will be stored at -80°C until analysis. Beta-endorphin concentrations will be determined using a commercially available ELISA kit.

    Time frame: Baseline and week 4

07

Study locations

1 of 1 sites recruiting
  • Gül DURAL
    Elâzığ, Turkey (Türkiye)
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07524231
Lead sponsor
Firat University
Responsible party
Gul Dural (Assistant professor, Firat University) — Principal investigator
First posted
Apr 13, 2026
Start date
Mar 10, 2026
Primary completion
Jul 10, 2026 (estimated)
Completion
Aug 10, 2026 (estimated)
Last update
Apr 13, 2026

Study contacts

Gül DURAL, pHD
Contact
gulkaya@firat.edu.tr
04242370000

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion