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
1 other identifier
interventional
36
1 country
1
Brief Summary
Purpose of the study; The aim of this study is to examine the effect of a compassion-based education program applied to mothers of children with cerebral palsy on compassion fatigue, depression, and psychological resilience.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2023
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
August 2, 2023
CompletedStudy Start
First participant enrolled
September 1, 2023
CompletedFirst Posted
Study publicly available on registry
February 7, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 14, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2024
CompletedFebruary 7, 2024
January 1, 2024
6 months
August 2, 2023
January 30, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Assessment and Evaluation of Depression
Burns Depression Scale will be applied to all participants. Depression levels will be determined.
Day 1
Assessment and Evaluation of Psychological Resilience
Psychological Resilience Scale for Adults will be applied to all participants. Psychological Resilience levels will be determined.
Day 1
Assessment and Evaluation of Compassion
Compassion Scale will be applied to all participants. Compassion levels will be determined .
Day 1
Secondary Outcomes (3)
The last test of Assessment and Evaluation of Depression
through study completion, an average of 1 week.
The last test of Assessment and Evaluation of Psychological Resilience
through study completion, an average of 1 week.
The last test of Assessment and Evaluation Compassion
through study completion, an average of 1 week.
Study Arms (2)
Experimental Group
EXPERIMENTALParticipants who will receive the training
Control Group
NO INTERVENTIONparticipants who will not be interfered with
Interventions
Training will be given once a week. This training will last 10 weeks in total.
Eligibility Criteria
You may qualify if:
- Being the mother of a child with Cerebral Palsy
You may not qualify if:
- Mothers who have children with Cerebral Palsy do not want to participate in the study and want to leave the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hasan Kalyoncu University
Gaziantep, Central, 27100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director
Study Record Dates
First Submitted
August 2, 2023
First Posted
February 7, 2024
Study Start
September 1, 2023
Primary Completion
February 14, 2024
Study Completion
March 30, 2024
Last Updated
February 7, 2024
Record last verified: 2024-01
Data Sharing
- IPD Sharing
- Will not share