- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07421336
Effects of Laughter Yoga in Older Adults
EFFECTS OF LAUGHTER YOGA ON PSYCHOLOGİCAL WELL-BEING AND DEPRESSIVE SYMPTOMS IN OLDER ADULTS
Study Overview
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Fatma Sena Albayrak
- Phone Number: +90 552-366-2976
- Email: senaalbayrak2976@gmail.com
Study Locations
-
-
-
Ankara, Turkey (Türkiye)
- Recruiting
- Ankara University Faculty of Nursing
-
Contact:
- Fatma Sena Albayrak, graduate student
- Phone Number: +90 552 366 2976
- Email: senaalbayrak2976@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Not having a diagnosis of neurocognitive disorders such as Alzheimer's or dementia.
- Not having a diagnosis of mental disorder
- Being 65 years and older
- Literacy
- Not having communication problems that would prevent answering the data collection form.
- Volunteering to participate in the research
Exclusion Criteria:
- Having a diagnosis of neurocognitive disorders such as Alzheimer's or dementia.
- Having a diagnosis of mental disorder
- Being under 60 years of age
- Illiteracy
- Having communication problems that prevent one from answering the data collection form.
- Not volunteering to participate in the research.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Laughter yoga
This group will undergo laughter yoga intervention.
|
The study divided the intervention and control groups. Participants in the intervention group will be given laughter yoga. Data collection tools will be administered as pre-tests to both the intervention and control groups. After the laughter yoga sessions are completed, data collection tools will be administered again as post-tests to both groups. |
|
No Intervention: control group
No intervention will be made against this group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
geriatric depression scale - short form
Time Frame: eight weeks
|
The scale consists of fifteen questions, which are answered with "yes/no".
The scale results indicate that a score of 0-4 does not indicate depression, 5-8 indicates mild depression, 9-11 indicates moderate depression, and 12-15 indicates severe depression.
|
eight weeks
|
|
Psychological Well-being Scale for the Elderly (YPİOÖ)
Time Frame: eight weeks
|
The scale, consisting of fifteen questions, is a 5-point Likert type. 1 point is answered as "strongly disagree" and 5 points as "strongly agree". Items 8 and 13 are reverse-scored. The minimum score on the scale is 15, and the maximum score is 75. According to the scores obtained from the scale, a score of 60-75 indicates high psychological well-being, a score of 45-59 indicates moderate psychological well-being, and a score of 15-44 indicates low psychological well-being. |
eight weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AnkaraU-SBE-FSA-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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