Implementation of the program based on transitional care model (TCM) on quality of life and activity of daily life of patients with stroke

Not Applicable

Recruiting

• Conditions: Stroke.; Cerebellar stroke syndrome; G46.4

• Registration Number: IRCT20190712044181N3
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

The diagnosis of stroke was confirmed by a neurologist who was selected to be a resident of the study group in Isfahan.
Willingness to participate in the study.
Be hospitalized for the first time with a stroke diagnosis.
Phone number to call.
Patients with at least GCS 13-15.
Patients selected for the study group reside in Isfahan.

Exclusion Criteria

The patient should not have a decreased consciousness.
Has no other neurological or mental illness. Has been hospitalized for the first time with a stroke diagnosis
The patient has not undergone skull or brain surgery.
Patients with perceptual or global aphasia are not included in the study.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcome measure of quality of life in stroke patients. Timepoint: Before the intervention (pre-test), after the intervention in the tenth week after discharge (post-test). Method of measurement: Specific standard questionnaire for quality of life after stroke (SS-QOL).;The ability to perform daily living activities in stroke patients. Timepoint: Before the intervention (pretest), after the intervention in the tenth week after discharge (post-test). Method of measurement: Barthel questionnaire will be used.