NCT07577024

Brief Summary

The effect of laughter yoga on a child's pre-operative anxiety.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 13, 2026

Completed
28 days until next milestone

First Posted

Study publicly available on registry

May 11, 2026

Completed
Last Updated

May 22, 2026

Status Verified

October 1, 2025

Enrollment Period

2 months

First QC Date

April 13, 2026

Last Update Submit

May 18, 2026

Conditions

Keywords

laughter yogachildrenpre-operative anxiety

Outcome Measures

Primary Outcomes (1)

  • pre-operative anxiety

    modified Yale Preoperative Anxiety Scale (mYPAS scale) will be applied.

    First arrival at the preoperative area, 10 minutes after laughter yoga.

Study Arms (2)

Intervention Group

EXPERIMENTAL

The group receiving laughter therapy.

Other: laughter therapy

Control Group

NO INTERVENTION

The group receiving routine services.

Interventions

Within the scope of the study, children in the intervention group-who are brought to the preoperative area one hour in advance as per routine practice-will be administered a pre-test by a blinded nurse researcher, followed by a laughter yoga session conducted by the researcher lasting approximately 30 minutes. To allow the physiological and psychological effects of the intervention to stabilize, the post-test will be administered 10 minutes after the session. In the control group receiving routine care without laughter yoga, the pre-test will be administered, and a post-test will be performed after a 40-minute waiting period to ensure consistency in the time criteria between the two groups.

Intervention Group

Eligibility Criteria

Age5 Years - 12 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Speaking Turkish
  • Having American Society of Anesthesiologists (ASA) I and II certifications
  • Planned as an elective operation
  • Children aged 5-12 undergoing their first surgery
  • Having no chronic illnesses

You may not qualify if:

  • Children with accompanying chronic illnesses and/or psychological disorders
  • Children with health problems that prevent them from doing laughter yoga (urinary incontinence, persistent cough, etc.)
  • Parents and children who refuse to participate in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Etlik city hospital

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Laughter Therapy

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeutics

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 13, 2026

First Posted

May 11, 2026

Study Start

January 1, 2026

Primary Completion

February 28, 2026

Study Completion

February 28, 2026

Last Updated

May 22, 2026

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Data are available from the corresponding author upon reasonable request

Locations