The Knowledge Gaps of Amputee Rehabilitation Course Content in Physiotherapy Curriculum

August 22, 2024 updated by: Hatice Gül, Akdeniz University

The Knowledge Gaps of Amputee Rehabilitation Course Content in Physiotherapy Curriculum According to International Classification of Functioning, Disability and Health (ICF)

Understanding the knowledge gaps of amputee rehabilitation course content is essential for addressing these gaps. Identifying the course contents according to International Classification of Functioning, Disability and Health (ICF) can be a starting point for determining the gaps. This study aimed to investigate which amputee-specific ICF categories are underemphasized in the course content.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

For understanding the knowledge gaps of amputee rehabilitation course content, a total of 59 amputee-specific ICF categories were asked to the academics whether these categories are present in the amputee rehabilitation course content. Academics were asked to answer "yes" or "no" to each question. Cochrane Q test was used to test for differences between the frequencies of ICF categories.

Sleep functions, high-level cognitive functions in the field of body functions, writing and handling stress in the activity sub-domain, most of the categories in the participation sub-domain and environmental factors were significantly underemphasized in the course content.This study identifies the knowledge gaps of amputee rehabilitation course content in physiotherapy curriculum.

Study Type

Observational

Enrollment (Actual)

73

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

      • Antalya, Turkey
        • Akdeniz University

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Academicians aged 25-80 and continued to teach amputee rehabilitation in different higher education institutions in Turkey were included in the study.

Description

Inclusion Criteria:

  • Academicians who continued to teach amputee rehabilitation in different higher education institutions in Turkey were included in the study.

Exclusion Criteria:

  • Individuals who did not teach the whole course but contributed to only a part of it were not included in 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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
1
Academicians who continued to teach amputee rehabilitation in different higher education institutions in Turkey were included in the study.

The survey was developed using the Google Forms platform. The first part of the questionnaire consisted of descriptive information such as age, gender, duration of academic experience. In addition to this informations, the questionnaire also included information related the status of use ICF in any fields.

In the other part of the questionnaire, a total of 59 questions (16 related to body functions, 3 related to body structures, 30 related to activity and participation, 10 related to environmental factors) were asked to the academicians whether these categories are present in the amputee rehabilitation course content. Academicians were asked to answer "yes" or "no" to each question.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Survey
Time Frame: 1 day

The survey was developed using the Google Forms platform. The first part of the questionnaire consisted of descriptive information such as age, gender, duration of academic experience. In addition to this informations, the questionnaire also included information related the status of use ICF in any fields.

In the other part of the questionnaire, a total of 59 questions (16 related to body functions, 3 related to body structures, 30 related to activity and participation, 10 related to environmental factors) were asked to the academicians whether these categories are present in the amputee rehabilitation course content. Academicians were asked to answer "yes" or "no" to each question.

1 day

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hatice Gül, Akdeniz University Vocational School of Health Services

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

February 1, 2024

Primary Completion (Actual)

May 30, 2024

Study Completion (Actual)

May 30, 2024

Study Registration Dates

First Submitted

August 16, 2024

First Submitted That Met QC Criteria

August 22, 2024

First Posted (Actual)

August 26, 2024

Study Record Updates

Last Update Posted (Actual)

August 26, 2024

Last Update Submitted That Met QC Criteria

August 22, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 202391-12/12/2023

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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