NCT06022172

Brief Summary

Cerebral palsy (CP) is a non-progressive problem that occurs as a result of damage or lesion in the brain tissue in the prenatal, perinatal or postnatal periods for any reason, causing permanent impairment in the development of posture and movement. In addition to the impairments in the motor area in CP; It can be seen in problems such as perception, cognitive, sensory, communication, social, behavioral, musculoskeletal, epilepsy .Parents who are primary caregivers of the child with CP; They have a very important caregiver role in meeting the processes such as the treatment of the child, daily life needs and rehabilitation.Parental self-efficacy has been defined as the judgments and beliefs held by the parents to cope with the difficulties they experience in raising and caring for children with developmental disabilities and to reach the goal.The long process of caring for the child with cerebral palsy and the dependence of the child on the parent increase the stress of the caregivers. The Calgary Family Intervention Model (CAMM), one of the nursing models, is the first family intervention model in the field of nursing. The model focuses on improving, developing and maintaining the family's functionality in three areas. These three areas are cognitive, emotional and behavioral.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 14, 2023

Completed
18 days until next milestone

First Posted

Study publicly available on registry

September 1, 2023

Completed
9 days until next milestone

Study Start

First participant enrolled

September 10, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 10, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2023

Completed
Last Updated

September 22, 2023

Status Verified

September 1, 2023

Enrollment Period

1 month

First QC Date

August 14, 2023

Last Update Submit

September 21, 2023

Conditions

Keywords

SP Ebeveyn Calgary Model Bakım Verme Öz-Yeterlik Stres

Outcome Measures

Primary Outcomes (2)

  • Pre-test data collection

    The research pre-test data will be carried out by the researcher between September 2023 and October 2023 in the interview rooms of rehabilitation centers, with the parents of children with cerebral palsy attending a private rehabilitation center in Iğdır. Introductory information form The burden of care for individuals in the experimental and control groups in data collection, parent self-efficacy scale and coping styles scale will be applied. In the care burden scale, a minimum score of 0 and a maximum of 88 points can be obtained from the scale. The lowest score in the self-efficacy scale is 17 and the highest score is 119. In the scale of coping with stress, the total score is calculated is not done.

    Time frame 1 or 2 months.

  • Collection of post-test data

    The motivational interview based on the Calgary family intervention model for each parent in the experimental group will consist of 6 sessions lasting 45 minutes, one week apart. After the interviews, the final test will be held after the last session and 15 days later. Parents of children with cerebral palsy whose children attend a special rehabilitation center in Istanbul will meet in the meeting rooms of the rehabilitation centers. Introductory information form, caregiver burden scale, parent self-efficacy scale and coping styles scale will be used to collect data. A score of 88 can be obtained. The lowest score in the self-efficacy scale is 17, and the highest score is 119. The total score is not calculated in the scale of coping with stress.

    Time frame one or two months.

Study Arms (2)

Experimental group

EXPERIMENTAL

MOTIVATIONAL INTERVIEW BASED ON THE CALGARY FAMILY INTERVENTION MODEL IN PARENTS WITH A CHILD WITH CEREBRAL PALS.

Diagnostic Test: MOTIVATIONAL INTERVIEW BASED ON THE CALGARY FAMILY INTERVENTION MODEL IN PARENTS WITH A CHILD WITH CEREBRAL PALS.

CONTROL GROUP

NO INTERVENTION

no action will be taken

Interventions

Motivational interview based on Calgary family intervention model in parents of children with cerebral palsy. Introductory information form, caregiving burden, parent self-efficacy and stress coping styles scale will be used.

Experimental group

Eligibility Criteria

Age6 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Having a child with cerebral palsy between the ages of 6-18,
  • Able to read and write Turkish, accessible and able to communicate,
  • Orientation and cooperation
  • Hearing, comprehension and vision problems,
  • Parents who agreed to participate in the study were determined as .

You may not qualify if:

  • Having difficulty in communication
  • Not being literate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Igdir university

Iğdır, 76000, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Cerebral Palsy

Condition Hierarchy (Ancestors)

Brain Damage, ChronicBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Study Officials

  • Gülçin Aşut, Doctorate

    Igdir University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Gülçin AŞUT, Doctorate

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: 30 people in the experimental group and 30 people in the control group, a total of 60 people will be included in the study
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Teaching Assistant

Study Record Dates

First Submitted

August 14, 2023

First Posted

September 1, 2023

Study Start

September 10, 2023

Primary Completion

October 10, 2023

Study Completion

December 30, 2023

Last Updated

September 22, 2023

Record last verified: 2023-09

Locations