Actively Recruiting

Age: 18Years - 75Years
All Genders
ID07228754

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

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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

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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

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