Study of the Effect of Compassion-Based Education Program Applied to Mothers of Children Diagnosed With Cerebral Palsy

January 30, 2024 updated by: Murat SEVEN, Hasan Kalyoncu University

Investigation of the Effect of Compassion-Based Education Program Applied to the Mothers of Children Diagnosed With Cerebral Palsy on Compassion, Depression and Resilience

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.

Study Overview

Status

Recruiting

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

Interventional

Enrollment (Estimated)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Turkey
    • Central
      • Gaziantep, Central, Turkey, 27100
        • Recruiting
        • Hasan Kalyoncu University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Other: Compassion-Based Education Program Adapted for Adults
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

This is where you will find people and organizations involved with this study.

Sponsor

Hasan Kalyoncu University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2023

Primary Completion (Estimated)

February 14, 2024

Study Completion (Estimated)

March 30, 2024

Study Registration Dates

First Submitted

August 2, 2023

First Submitted That Met QC Criteria

January 30, 2024

First Posted (Estimated)

February 7, 2024

Study Record Updates

Last Update Posted (Estimated)

February 7, 2024

Last Update Submitted That Met QC Criteria

January 30, 2024

Last Verified

January 1, 2024

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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