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

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:

  1. Followed by ischemic or hemorrhagic stroke
  2. No more than 6 months have passed since the date of the event
  3. Being between the ages of 18 and 75
  4. The caregiver being between the ages of 18 and 75

Exclusion Criteria:

  1. The patient has additional neurological conditions besides stroke
  2. The patient has a psychiatric condition
  3. 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.

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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