- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05351528
of Caregiver Family Members for the Disabled in Bukhara
April 22, 2022 updated by: Nurhayat KORKMAZ, Karadeniz Technical University
Relationship Between Burdens and Healthy Lifestyle Behaviors of Caregiver Family Members for the Disabled in Bukhara
The responsibilities of caring for a disabled family member may cause caregivers to develop risky behaviors for caregiver's health.
Therefore, we aimed to examine the relationship between caregiver burdens and healthy lifestyle behaviors of family members caring for a disabled child.
Study Overview
Detailed Description
In the study, family members living in Bukhara, Uzbekistan, and caring for a disabled person under the age of 24 were evaluated.
Caregiver burden was evaluated with the Caregiver Burden Scale and healthy lifestyle behaviors were evaluated with the Healthy Lifestyle Behaviors Scale II.
The fact that there is no earlier study on caregivers of disabled people in Uzbekistan and no research in the literature examining the relationship between caregiving burden and healthy lifestyle behaviors in individuals with disabled children, make this study unique.
Study Type
Observational
Enrollment (Actual)
155
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
-
-
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Trabzon, Turkey, 61000
- Karadeniz Technical University
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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
- CHILD
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Caregiver Family Member with disabled children
Description
Inclusion Criteria:
- Volunteering to participate in the study
- Having a disabled child to take care of
- Being literate
Exclusion Criteria:
- The age of the disabled person being cared for is over 24 years old.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Socio-demographic information
Time Frame: Two months
|
Age, height, body weight, employment status, income status, marital status
|
Two months
|
|
Number of child
Time Frame: Two months
|
Number of healthy and disabled children
|
Two months
|
|
Assessment of the child age
Time Frame: Two months
|
Age
|
Two months
|
|
Assessment of the child
Time Frame: Two months
|
Gender
|
Two months
|
|
Caregiver Burden Scale
Time Frame: Two months
|
The scale has a Likert-type rating ranging from 0 to 4 as "never, rarely, sometimes, quite often, almost always".
A minimum of 0 and a maximum of 88 points can be obtained from the scale.
The items in the scale are generally related to the social and emotional domain, and a high score indicates a high level of distress.
|
Two months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Healthy Lifestyle Behaviors Scale II
Time Frame: Two months
|
The scale is scored as "never (1)-regularly (4)".
The lowest score for the whole scale is 52 and the highest score is 208.
The high scores obtained from the scale indicate how high the individual applies the specified health behaviors.
|
Two months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 26, 2021
Primary Completion (ACTUAL)
December 30, 2021
Study Completion (ACTUAL)
March 30, 2022
Study Registration Dates
First Submitted
April 11, 2022
First Submitted That Met QC Criteria
April 22, 2022
First Posted (ACTUAL)
April 28, 2022
Study Record Updates
Last Update Posted (ACTUAL)
April 28, 2022
Last Update Submitted That Met QC Criteria
April 22, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KTU-SBU-FTR-01
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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