- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07228754
How Realistic Are Caregivers' Expectations in Patients With Subacute Stroke?
February 22, 2026 updated by: Ayse Naz Kalem, Ankara Etlik City Hospital
How Realistic Are Caregivers' Expectations in Determining Rehabilitation Goals for Subacute Stroke Patients?
The aim of this study is to evaluate the extent to which the patient's goals and the physical therapist's goals can be achieved after stroke rehabilitation and to compare their expectations in terms of rehabilitation outcomes.
Thus, the expected benefit of the study is to contribute to goal setting in post-stroke rehabilitation.
There are no expected risks from the study.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
58
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ayse Naz Kalem Ozgen, Specialist
- Phone Number: +90 0312 797 00 00
- Email: kalemnaz@gmail.com
Study Locations
-
-
Yenimahalle
-
Ankara, Yenimahalle, Turkey (Türkiye), 06010
- Recruiting
- Ankara Etlik City Hospital
-
Contact:
- Ayse Naz Kalem Ozgen, Specialist
- Phone Number: +90 0312 797 00 00
- Email: kalemnaz@gmail.com
-
-
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
No
Sampling Method
Probability Sample
Study Population
Fifty-eight stroke patients receiving inpatient treatment at the Ankara Etlik City Hospital Brain Injury-3 clinic and their caregivers will be evaluated.
Description
Inclusion Criteria:
- Followed by ischemic or hemorrhagic stroke
- No more than 6 months have passed since the date of the event
- Being between the ages of 18 and 75
- The caregiver being between the ages of 18 and 75
Exclusion Criteria:
- The patient has additional neurological conditions besides stroke
- The patient has a psychiatric condition
- The patient is not willing to participate 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 |
|---|---|
|
Stoke Patients
|
Conventional rehabilitation programme described for patients individually
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Goal Attainment Scale
Time Frame: First day of rehabilitation, 4th week of rehabilitation
|
The Goal Attainment Scale will be used as the primary outcome measure within the framework of goals set separately by the caregiver and the physical therapist.
|
First day of rehabilitation, 4th week of rehabilitation
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Functional Ambulation Scale
Time Frame: First day of rehabilitation, 4th week of rehabilitation
|
First day of rehabilitation, 4th week of rehabilitation
|
|
Modified Barthel Index
Time Frame: First day of rehabilitation, 4th week of rehabilitation
|
First day of rehabilitation, 4th week of rehabilitation
|
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)
December 6, 2025
Primary Completion (Estimated)
May 1, 2026
Study Completion (Estimated)
May 1, 2026
Study Registration Dates
First Submitted
November 13, 2025
First Submitted That Met QC Criteria
November 13, 2025
First Posted (Actual)
November 14, 2025
Study Record Updates
Last Update Posted (Actual)
February 24, 2026
Last Update Submitted That Met QC Criteria
February 22, 2026
Last Verified
November 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- AEŞH-BADEK1-2025-479
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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