How Realistic Are Caregivers' Expectations in Patients With Subacute Stroke?
NCT ID: NCT07228754
Last Updated: 2025-11-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
58 participants
OBSERVATIONAL
2025-11-06
2026-05-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Cardiopulmonary Rehabilitation in Chronic Stroke
NCT03558542
Effects of Robot-Assisted Upper Extremity Training on Cognitive and Physical Functions After Stroke
NCT04335422
Activity Daily Living Performance in Patients With Stroke
NCT03723213
Turkish Adaptation, Validity, and Reliability Study of the Patient Experience With Treatment and Self-Management Scale in Stroke
NCT07253506
Comparison of the Effects of Cycling FES and Conservative Rehabilitation Therapy on Stroke Patients
NCT05667025
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Stoke Patients
Conventional rehabilitation programme
Conventional rehabilitation programme described for patients individually
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Conventional rehabilitation programme
Conventional rehabilitation programme described for patients individually
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
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
2. The patient has a psychiatric condition
3. The patient is not willing to participate in the study
18 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ankara Etlik City Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ayse Naz Kalem
PM&R Specialist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ankara Etlik City Hospital
Ankara, Yenimahalle, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AEŞH-BADEK1-2025-479
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.