Study of the Effect of Compassion-Based Education Program Applied to Mothers of Children Diagnosed With Cerebral Palsy
Investigation of the Effect of Compassion-Based Education Program Applied to the Mothers of Children Diagnosed With Cerebral Palsy on Compassion, Depression and Resilience
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The Hypotheses of the Study
Main Hypothesis: "Compassion-Based Education Program Adapted for Adults" in increasing the compassion levels and psychological resilience of mothers of patients with CP; It is effective in reducing the level of depression.
As sub-hypotheses:
H1: The scores of the mothers who care for their children with Cerebral Palsy in the experimental group at the end of the application (post-test) and after the application (follow-up test) of the Adult Compassion Scale are significantly higher than the scores they obtained before the application (pre-test).
H2: The scores of the mothers who care for their children with Cerebral Palsy in the experimental group at the end of the application (post-test) and after the application (follow-up test) of the Burns Depression Scale-Turkish Form are significantly lower than the scores they obtained before the application (pre-test).
H3: The scores of the mothers who care for their children with Cerebral Palsy in the experimental group at the end of the application (post-test) and after the application (follow-up test) of the Adult Resilience Scale are significantly higher than the scores they obtained before the application (pre-test).
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Murat SEVEN, 1
- Phone Number: +90-501-131-8007
- Email: murat.seven@std.hku.edu.tr
Study Contact Backup
- Name: Sezer AVCI, 1
- Phone Number: +90-506-856-0446
- Email: sezer.avci@hku.edu.tr
Study Locations
-
-
Central
-
Gaziantep, Central, Turkey, 27100
- Recruiting
- Hasan Kalyoncu University
-
Contact:
- Sezer Avcı, 1
- Phone Number: +90-506-856-0446
- Email: sezer.avci@hku.edu.tr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being the mother of a child with Cerebral Palsy
Exclusion Criteria:
- Mothers who have children with Cerebral Palsy do not want to participate in the study and want to leave the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
Participants who will receive the training
|
Training will be given once a week.
This training will last 10 weeks in total.
|
|
No Intervention: Control Group
participants who will not be interfered with
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment and Evaluation of Depression
Time Frame: Day 1
|
Burns Depression Scale will be applied to all participants.
Depression levels will be determined.
|
Day 1
|
|
Assessment and Evaluation of Psychological Resilience
Time Frame: Day 1
|
Psychological Resilience Scale for Adults will be applied to all participants.
Psychological Resilience levels will be determined.
|
Day 1
|
|
Assessment and Evaluation of Compassion
Time Frame: Day 1
|
Compassion Scale will be applied to all participants.
Compassion levels will be determined .
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The last test of Assessment and Evaluation of Depression
Time Frame: through study completion, an average of 1 week.
|
Burns Depression Scale will be applied to all participants.
Depression levels will be determined due to showing effectiveness of training.
|
through study completion, an average of 1 week.
|
|
The last test of Assessment and Evaluation of Psychological Resilience
Time Frame: through study completion, an average of 1 week.
|
Psychological Resilience Scale will be applied to all participants.
Resilience levels will be determined due to showing effectiveness of training.
|
through study completion, an average of 1 week.
|
|
The last test of Assessment and Evaluation Compassion
Time Frame: through study completion, an average of 1 week.
|
Compassion Scale will be applied to all participants.
Compassion levels will be determined due to showing effectiveness of training.
|
through study completion, an average of 1 week.
|
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 (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MSEVEN
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
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