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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06457061
Other study ID # AIBU-FTR-SK-06
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2023
Est. completion date May 1, 2024

Study information

Verified date June 2024
Source Abant Izzet Baysal University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aimed to evaluate the caregiving burden and severity of depression in patients with right hemiplegia and left hemiplegia.


Description:

Stroke is a disease characterized by neurological symptoms and signs lasting more than 24 hours, which can lead to death after the interruption of brain blood flow or due to focal brain damage. Post-stroke disability affects the patient's quality of life, makes the patient dependent on the caregiver, creates a caregiver burden, and brings socioeconomic and social consequences. Different hemispheres of the brain undertake different tasks. Different clinical conditions may occur in stroke patients with right or left hemiplegia following cerebrovascular infarction. This may affect the care burden of caregivers and the severity of depression. It was thought that knowing the care burden of patients with right and left hemiplegia would positively contribute to the quality of care given to patients.This study aimed to evaluate the caregiving burden and severity of depression in patients with right hemiplegia and left hemiplegia.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Hemiplegia patients between the ages of 18 and 75 were included. - Caregivers over 18 years of age - At least 3 months must have passed since the patient was diagnosed. - Caregivers of patients should be their first and second degree relatives. - Caregivers must be competent to understand what they read and complete the questionnaires. - Caregivers must have been caring for their patients for at least 3 months. Exclusion Criteria: - Patients and caregivers with a history of psychiatric illness

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey Study
Barthel Index for Activities of Daily Living Scale, Beck Depression Inventory and Star Cancellation Test questionnaires were applied to hemiplegia patients. Beck Depression Inventory and Zarit Caregiver Burden Interview surveys were administered to caregivers.

Locations

Country Name City State
Turkey Abant Izzet Baysal University Bolu

Sponsors (1)

Lead Sponsor Collaborator
Abant Izzet Baysal University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Beck's Depression Inventory The Beck Depression Inventory (BDI) is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression. The score to be received varies between 0-63. A high total score indicates a higher severity of depression. Day 1
Primary Zarit Caregiver Burden Zarit caregiver burden interview evaluates caregivers' caregiving burden. It consists of 22 questions. A minimum of 0 and a maximum of 88 points can be obtained from the scale. A A high total score indicates a higher severity of caregiver burden Day 1
Secondary Barthel Index for Activities of Daily Living Scale The Barthel index is used to assess activities of daily living. It consists of 10 items: feeding, bathing, grooming, dressing, bowel, bladder, toilet use, transfers, mobility, stairs. Scores range from 0-100. A score of 100 represents complete independence, and a score of 0 represents complete dependence. Day 1
Secondary Star Cancellation test The Star Cancellation Test is a screening tool developed to detect the presence of unilateral spatial neglect Day 1
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