- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04170569
Yoga on Posttraumatic Growth and Quality of Life
The Effect of Yoga on Posttraumatic Growth and Quality of Life in the Postpartum Period
The objective of this study is to examine the effect of yoga on posttraumatic growth and quality of life. The birth action, which includes positive and negative experiences, can be an important opportunity to achieve posttraumatic growth and improve the quality of life.
This is a experimental model with pretest-posttest control group study. Two hundred and fifty-two women who met the criteria for inclusion in the study made up the research population. Three instruments were used to obtain the research data: Personal Information Form, Posttraumatic Growth Inventory (PTGI) and SF-36 Quality of Life Questionnaire (SF-36).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Failure in modern medicine approaches or side effects of treatments and drugs, as well as the woman's anxiety to hurt herself and her baby direct her and her relatives to try complementary therapies. Women should prefer natural ways in coping with these postpartum problems rather than seeking medical advice.
When yoga and meditation, which are included in the group of mind-body-based complementary therapies, are performed in the postpartum period, they will help to relieve tensions and distresses that accumulate during birth, strengthen the pelvic floor, heal perineum, bring reproductive organs back to their prepregnancy condition healthily, provide the mother and the infant a sleep pattern, and have an easier transition to sleep.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Battalgazi
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Malatya, Battalgazi, Turkey, 44100
- Hacer
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Having a baby between 2 and 6 months
- First time mom
- No tissue deformity in extremities
Exclusion Criteria:
- Any gynecological disease
- Any psychiatric illness
- Using any psychiatric medication
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: Experimental Group
Yoga program was applied.
|
Yoga Practice and Program: Yoga practice consisted of 10 weeks.
Yoga practice involved following stages; 5-minute breathing exercises in standing or sitting position, 40-minute postpartum period specific asanas and last 15- minute deep relaxation in lying position were made by the researcher.
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No Intervention: Control Group
No yoga program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Effect of Yoga on Posttraumatic Growth in the Postpartum Period
Time Frame: 10 weeks
|
The posttraumatic growth scale for measure posttraumatic growth;The scale is scored from 0 to 5 and the lowest is 0 and the highest is 105.
The higher the scores obtained, the higher the approval from the traumatic experience shows that it is experiencing high growth.
There are three sub-dimensions: the change in self-perception of the scale, the change in philosophy of life, and the change in relationship with others.
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10 weeks
|
The Effect of Yoga on Quality of Life in the Postpartum Period
Time Frame: 10 weeks
|
SF-36 Quality of life scale for measure the quality of life; The scale is calculated by inverting the items 1, 6, 7, 8, 9d, 9e, 9h, 11b, 11d.
Total score is not calculated in the scale.
The subscales evaluate health between 0-100 points.
0 indicates "poor health" and 100 indicates "good health.Higher scores obtained from the subscales of the scale indicate that the quality of life level is high.
|
10 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- Inonu University.
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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