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NCT07504848Completed

Stroke Mobility and Caregiver Outcomes

The Effect of Mobility Level in Stroke Patients on Anxiety, Depression, and Caregiver Burden in Caregivers

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

This study was designed to determine the effect of functional mobility levels of stroke patients on caregiver burden, anxiety, and depression in their caregivers.

Status (registry)
Completed
Study type
Observational
Enrollment
64 (actual)
First submitted
26 Mar 2026
Start date
2 Apr 2026
Primary completion date
15 Apr 2026
Lead sponsor
Ondokuz Mayıs University
Diseases
Stroke
NCT number
NCT07504848

What you commit to

  • Study type: Observational
  • Participants enrolled: 64
  • From 2 Apr 2026 to the primary completion date, 15 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Stroke Patients:
    • Presence of severe comorbid conditions
    • Unwillingness to participate
    • History of multiple strokes
    • Bilateral hemiplegia
    • Presence of major neurological, orthopedic, or rheumatologic disorders affecting the musculoskeletal system other than stroke
    • Congenital anomalies or amputation causing disability
    • Uncontrolled arrhythmia, uncontrolled hypertension, or unstable cardiac conditions
    • Botulinum toxin injection within the last 6 months
    • Inability to establish cooperation
    • Presence of neglect, aphasia, or hemianopsia
  • Caregivers of Stroke Patients:
    • Unwillingness to participate
    • Living with the patient for less than 1 year
    • Presence of mental retardation, dementia, or severe psychotic disorders

Who the study is looking for

  • Stroke Patients:
    • Diagnosed with stroke according to WHO criteria (≥20% disability rate documented in Adult Disability Health Board Report)
    • Having a family member or relative who provides care
    • First-ever and unilateral stroke
    • Willing to participate voluntarily
    • Aged between 18-75 years
    • Post-stroke duration longer than 3 months
    • Stable vital signs
    • Scoring ≥24 on the Standardized Mini-Mental State Examination (SMMT) or the -Modified Mini-Mental State Examination for Illiterate Individuals (MMSE-E)
    • Able to understand and speak Turkish
  • Caregivers of Stroke Patients:
    • Willing to participate in the study
    • Living with the patient for at least 1 year
    • Being the primary (main responsible) caregiver and not receiving paid professional caregiving services
    • Aged 18 years or older
    • Scoring ≥24 on the Standardized Mini-Mental State Examination (SMMT) or MMSE-E

Age in the registry: 18 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ondokuz Mayis University
Coordinator of this site? Confirm its status
SamsunTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.