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StrokeNCT07228754

How Realistic Are Caregivers' Expectations in Patients With Subacute Stroke?

An observational study of Stroke, run by Ankara Etlik City Hospital at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aims to compare rehabilitation goals independently established by caregivers of patients with stroke and physiatrists, and to evaluate the extent to which these goals are achieved following rehabilitation. Read more about this study

Who is it for?
Ages 18 to 75 yearsHealthy volunteers can take part
Conditions the study is for
Stroke
What is being tested?
Conventional rehabilitation programme
How many people
58 participants
Where
1 siteTurkey (Türkiye)
Study dates
6 Dec 2025to 1 Oct 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Fifty-eight stroke patients receiving inpatient treatment and fifty-eight caregivers at the Ankara Etlik City Hospital will be evaluated.

Who may be able to join

  • Diagnosis of ischemic or hemorrhagic stroke.
  • Stroke onset within the previous 6 months.
  • Being between 18 and 75 years of age.
  • Participation in an inpatient stroke rehabilitation program.
  • Being between 18 and 75 years of age.
  • Being a family member or primary caregiver of a patient with stroke enrolled in the study.
  • Having provided care to the patient with stroke for at least one month.
  • Willingness to participate in the study.

Who cannot join

  • Presence of additional neurological conditions other than stroke that may affect functional recovery.
  • Presence of a psychiatric condition that may interfere with participation in the study.
  • Unwillingness to participate in the study.
  • Caregivers of Patients with Stroke
  • Presence of a neurological or psychiatric condition that may interfere with understanding or completing the study assessments.
  • Cognitive or communication difficulties that prevent the independent establishment of rehabilitation goals using Goal Attainment Scaling (GAS).
  • Unwillingness to participate in the study.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Ankara Etlik City Hospital

    Ankara, Yenimahalle, 06010

Other trials in Turkey (Türkiye)

About this study

Official title: How Realistic Are Caregivers' Expectations in Determining Rehabilitation Goals for Subacute Stroke Patients?

This study aims to compare rehabilitation goals independently established by caregivers of patients with stroke and physiatrists, and to evaluate the extent to which these goals are achieved following rehabilitation. Goal attainment will be assessed using Goal Attainment Scaling (GAS), while functional independence and ambulatory function will be evaluated using the Barthel Index (BI) and Functional Ambulation Classification (FAC), respectively, at admission and discharge. The study is expected to provide insights into differences between caregiver and physiatrist expectations and contribute to more individualized and realistic goal setting in stroke rehabilitation.

Read the detailed description

The aim of this study is to evaluate and compare the rehabilitation goals and expectations of caregivers of patients with stroke and their physiatrists, and to assess the extent to which these goals are achieved following rehabilitation. At the beginning of the rehabilitation program, caregivers and physiatrists will independently establish their rehabilitation goals, allowing the identification of potential differences in their expectations and priorities.

Goal attainment will be assessed using Goal Attainment Scaling (GAS), which enables the evaluation of individualized rehabilitation goals and the extent to which they are achieved. At the end of the rehabilitation program, the achievement of caregiver-defined and physiatrist-defined goals will be evaluated separately and compared.

Additionally, functional independence in activities of daily living will be assessed using the Barthel Index (BI), while ambulatory function will be evaluated using the Functional Ambulation Classification (FAC). Both assessments will be performed at admission and discharge to determine functional improvements during rehabilitation. The relationship between goal attainment and functional outcomes will also be investigated.

The study is expected to contribute to a better understanding of differences between caregiver and physiatrist expectations, facilitate the establishment of realistic and individualized rehabilitation goals, and improve communication and shared decision-making in stroke rehabilitation. Furthermore, identifying potential discrepancies between goal achievement and objectively measured functional improvements may provide valuable insights for optimizing rehabilitation strategies and promoting caregiver involvement in the rehabilitation process.

No significant risks are anticipated from participation in this study, as no additional invasive procedures or interventions beyond routine rehabilitation assessments are planned.

Conditions
Stroke
Being tested
Conventional rehabilitation programme
Medical subject headings
Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Conventional rehabilitation programmeOther

    Conventional rehabilitation programme described for patients individually

Study groups in NCT07228754
Study groupRoleWhat they receive
Stroke PatientsCaregivers of patients with stroke will independently establish individualized rehabilitation goals using Goal Attainment Scaling (GAS) at the beginning of the rehabilitation program. These goals will reflect caregivers' expectations and priorities regarding the patients' functional recovery. At 4th week, the extent to which the predefined goals have been achieved will be assessed using GAS.
Receives: Other: Conventional rehabilitation programme

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Goal Attainment Scale - score for caregiver-set goals

    Goal Attainment Scaling (GAS) will be used to assess the extent to which individualized rehabilitation goals are achieved. Rehabilitation goals will be independently established by caregivers and physiatrists at the first day of the rehabilitation program. Goal attainment will be evaluated using a five-point scale ranging from -2 (much less than expected) to +2 (much better than expected), with 0 indicating the expected level of goal achievement. Higher scores indicate greater goal attainment.

    Measured: First day of rehabilitation, 4th week of rehabilitation

  2. Goal Attainment Scale - score for physiatrist-set goals

    Goal Attainment Scaling (GAS) will be used to assess the extent to which individualized rehabilitation goals are achieved. Rehabilitation goals will be independently established by caregivers and physiatrists at the first day of the rehabilitation program. Goal attainment will be evaluated using a five-point scale ranging from -2 (much less than expected) to +2 (much better than expected), with 0 indicating the expected level of goal achievement. Higher scores indicate greater goal attainment.

    Measured: First day of rehabilitation, 4th week of rehabilitation

Secondary outcomes (2)
  1. Functional Ambulation Category

    Functional Ambulation Category (FAC) will be used to assess walking ability and the level of physical assistance required for ambulation in patients with stroke. The scale consists of six levels ranging from 0 (nonfunctional ambulation) to 5 (independent ambulation on all surfaces), with higher scores indicating greater independence in walking.

    Measured: First day of rehabilitation, 4th week of rehabilitation

  2. Modified Barthel Index

    Modified Barthel Index (MBI) will be used to assess functional independence in activities of daily living in patients with stroke. The index evaluates 10 activities, including feeding, bathing, dressing, toileting, transfers, and mobility. Total scores range from 0 to 100, with higher scores indicating greater functional independence.

    Measured: First day of rehabilitation, 4th week of rehabilitation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Nov 2025
  2. Study start6 Dec 2025
  3. Primary completion1 Oct 2026
  4. Study completion1 Oct 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
58 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07228754
Sponsor's protocol ID
AEŞH-BADEK1-2025-479
Status last verified
Oct 2026
First submitted
13 Nov 2025
Last updated
2 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The data supporting this study's findings can be obtained from the corresponding author upon reasonable request.

Questions about this trial

What is this clinical trial studying?

An observational study of Stroke, run by Ankara Etlik City Hospital at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Goal Attainment Scale - score for caregiver-set goals (time frame: First day of rehabilitation, 4th week of rehabilitation). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Nov 2026.

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