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The Effect of Pre-rehabilitation and Rehabilitation Period on Functional Status in Inpatient Stroke Patients

Sponsor
Sisli Hamidiye Etfal Training and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05655039
Collaborator
(none)
108
Enrollment
1
Location
30
Actual Duration (Days)
109.6
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Patients who underwent inpatient rehabilitation for the last 5 years were retrospectively scanned. The pre-rehabilitation and rehabilitation periods of the patients were determined. At the beginning and end of rehabilitation, patients were evaluated with the Brunsstrom, Barthel and Stroke Impact Scale. The effect of the specified durations on these scales was investigated.

Condition or Disease Intervention/Treatment Phase
  • Other: Rehabilitation

Study Design

Study Type:
Observational
Actual Enrollment :
108 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
The Effect of Pre-rehabilitation and Rehabilitation Period on Functional Status in Inpatient Stroke Patients
Actual Study Start Date :
Sep 15, 2022
Actual Primary Completion Date :
Oct 15, 2022
Actual Study Completion Date :
Oct 15, 2022

Outcome Measures

Primary Outcome Measures

  1. Brunnsstrom Stages [immediately after Rehabilitation]

    The Brunnstrom stages of stroke recovery, or Brunnstrom approach, outlines how spasticity and involuntary motor patterns improve. Minimum score is 1, maximum score is 6. Higher score means better outcome.

  2. Barthel Index [immediately after Rehabilitation]

    The Barthel scale is an ordinal scale used to measure performance in activities of daily living. Each performance item is rated on this scale with a given number of points assigned to each level or ranking. It uses ten variables describing ADL and mobility. Minimum score is 0, maximum score is 100. Higher score means better outcome.

  3. Stroke Impact Scale [immediately after Rehabilitation]

    The Stroke Impact Scale (SIS) is a self-report questionnaire that evaluates disability and health-related quality of life after stroke. Minimum score is 0, maximum score is 100. Higher score means better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • 40-90 years old

  • Have hemodynamic stability to participate in rehabilitation

  • Having had an ischemic or hemorrhagic stroke

Exclusion Criteria:

  • Having a serious comorbidity that may preclude rehabilitation

  • Malignancy

  • Aphasia

  • Having a serious perception problem or psychiatric illness

  • Having a history of stroke

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Health Sciences, Şişli Hamidiye Etfal Training and Research Hospital Istanbul Turkey

Sponsors and Collaborators

  • Sisli Hamidiye Etfal Training and Research Hospital

Investigators

  • Study Director: Banu Kuran, Professor, Şişli Hamidiye Etfal Training and Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Aylin Ayyıldız, Director, Sisli Hamidiye Etfal Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT05655039
Other Study ID Numbers:
  • 2022
First Posted:
Dec 16, 2022
Last Update Posted:
Dec 16, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Stroke

Study Results

No Results Posted as of Dec 16, 2022