Turkish Adaptation of the Activity Limitations in Cerebral Palsy Questionnaire

January 8, 2022 updated by: Ilknur Naz, Izmir Katip Celebi University

Investigation of the Psychometric Properties of the Turkish Adaptation of the Activity Limitations in Cerebral Palsy Questionnaire

This study aimed to make the Turkish adaptation of ACTIVLIM-CP and to examine its psychometric properties. Eighty-nine individuals with CP, aged between 2-18 years were included in the study. PEDİ, ABILOCO-Kids, and ABILHAND-Kids scores and Wee-FIM questionnaires were used for validity analysis. Test re-test method was used for reliability.

Study Overview

Detailed Description

Cerebral Palsy (CP) is a clinical picture with permanent disorders of the development of movement and posture whether assessing activity limitations matters. This study aimed to make the Turkish adaptation of ACTIVLIM-CP and to examine its psychometric properties.

The internal consistency of the scale was evaluated using Cronbach's alpha value and the inter-measurement reliability using the intraclass correlation coefficient (ICC). In construct validity analysis; ACTIVLIM-CP score; was correlated with PEDİ, ABILOCO-Kids, and ABILHAND-Kids scores and Wee-FIM total scores. A known group comparison was made according to ambulation and epilepsy existence with the Principal Components Explanatory Factor Analysis.

Study Type

Observational

Enrollment (Actual)

89

Contacts and Locations

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

Study Locations

      • İzmir, Turkey, 35620
        • İlknur Naz Gürşan

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

2 years to 18 years (ADULT, CHILD)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

children with CP aged between 2 and 18 years and their parents

Description

Inclusion Criteria:

  • children with CP who were diagnosed by a child neurologist
  • having physical therapy sessions at special education and rehabilitation center
  • age between 2 and 18

Exclusion Criteria:

  • whose parent was illiterate or doesn't speak Turkish
  • whose parent wasn't complete the questionnaires

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Participants with CP
Children with CP
The ACTIVLIM-CP scale evaluates the global activity performance and combined movements of the body.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Global Activity Performance assessment
Time Frame: 15 minutes
ACTIVLIM-CP: Caregiver rates the difficulty degree of 43 activities easy/difficult/impossible/unknown). Questionnaire scores between 0 and 86 points. A higher score shows better activity performance
15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gunctional capabilities and limitations
Time Frame: 5 minutes
Gross Motor Function Classification System: It classifies the motor function of a child from level 1 (slightly affected) to level 5 (severely affected)
5 minutes
Functional independence measurement
Time Frame: 15 minutes
Functional Independence Measure for Children: The scale includes 18 measurement items and every item scores between 1 -7. A higher score shows more independence
15 minutes
Child's ability to walk assessment
Time Frame: 10 minutes
Abiloco-Kids: It consists of 10 questions for evaluating the walking performance from the viewpoint of the caregiver. Questionnaire scores between 0 and 20 points. A higher score shows better activity performance
10 minutes
child's manual ability assessment
Time Frame: 15 minutes
Abilhand-Kids: It consists of 21 questions to measure the manual ability from the viewpoint of the family. Questionnaire scores between 0 and 42 points. A higher score shows better activity performance.
15 minutes
Functional assessment
Time Frame: 20 minutes
Pediatric Evaluation of Disability Inventory (PEDI): It consists of three Functional Skills Scales, three Caregiver Assistance Scales, and three Modification Scales in the content areas of self-care, mobility, and social function. Functional Skills has 197 items and each item scores as 1(able) and 2(unable), Caregiver Assistance scores between 0(dependent) -5(independent) and Modifications assessing with frequencies .
20 minutes

Collaborators and Investigators

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

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)

December 1, 2020

Primary Completion (ACTUAL)

September 1, 2021

Study Completion (ACTUAL)

November 1, 2021

Study Registration Dates

First Submitted

December 22, 2021

First Submitted That Met QC Criteria

December 22, 2021

First Posted (ACTUAL)

January 11, 2022

Study Record Updates

Last Update Posted (ACTUAL)

January 25, 2022

Last Update Submitted That Met QC Criteria

January 8, 2022

Last Verified

December 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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