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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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06245733
Enrollment
36
Registered
2024-02-07
Start date
2023-09-01
Completion date
2024-03-30
Last updated
2024-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy

Keywords

Serebral Palsi, Depression, Resilience, Compassion

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.

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).

Interventions

OTHERCompassion-Based Education Program Adapted for Adults

Training will be given once a week. This training will last 10 weeks in total.

Sponsors

Hasan Kalyoncu University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Assessment and Evaluation of DepressionDay 1Burns Depression Scale will be applied to all participants. Depression levels will be determined.
Assessment and Evaluation of Psychological ResilienceDay 1Psychological Resilience Scale for Adults will be applied to all participants. Psychological Resilience levels will be determined.
Assessment and Evaluation of CompassionDay 1Compassion Scale will be applied to all participants. Compassion levels will be determined .

Secondary

MeasureTime frameDescription
The last test of Assessment and Evaluation of Depressionthrough 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.
The last test of Assessment and Evaluation of Psychological Resiliencethrough 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.
The last test of Assessment and Evaluation Compassionthrough 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.

Countries

Turkey (Türkiye)

Contacts

Primary ContactMurat SEVEN, 1
murat.seven@std.hku.edu.tr+90-501-131-8007
Backup ContactSezer AVCI, 1
sezer.avci@hku.edu.tr+90-506-856-0446

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026