Actively Recruiting
How Realistic Are Caregivers' Expectations in Determining Rehabilitation Goals for Subacute Stroke Patients?
Led by Ankara Etlik City Hospital · Updated on 2026-02-24
58
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are examining how well patients recovering from stroke and their physical therapists achieve their rehabilitation goals, and how realistic caregivers' expectations are regarding these outcomes. The study focuses on patients who have experienced ischemic or hemorrhagic stroke within the past six months. The goal is to improve the process of setting rehabilitation objectives for stroke survivors. Participants will undergo a conventional rehabilitation program tailored individually to each patient. The study will observe participants during the rehabilitation period, assessing progress at the start and after four weeks. Caregivers' expectations will be compared with actual rehabilitation results to understand alignment or differences. During the study, evaluations include the Goal Attainment Scale, Functional Ambulation Scale, and Modified Barthel Index measured on the first day and after four weeks of rehabilitation. Participants and their caregivers will be monitored closely to track rehabilitation progress, functional walking ability, and daily living activities. The study aims to contribute valuable insights into goal setting and rehabilitation planning for stroke patients over the course of these assessments.
CONDITIONS
Brief Title
How Realistic Are Caregivers' Expectations in Patients With Subacute Stroke?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Followed by ischemic or hemorrhagic stroke
- Stroke event occurred no more than 6 months ago
- Aged between 18 and 75 years
- Caregiver aged between 18 and 75 years
You will not qualify if you...
- Presence of additional neurological conditions besides stroke
- Having a psychiatric condition
- Not willing to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants who undergo conventional rehabilitation are observed to assess rehabilitation progress and caregivers' expectations.
2 visits (first day and 4th week of rehabilitation)
Trial Site Locations
Total: 1 location
1
Ankara Etlik City Hospital
Ankara, Yenimahalle, Turkey (Türkiye), 06010
Actively Recruiting
Research Team
A
Ayşe Naz Kalem Özgen, specialist
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here