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Effects of a Self-Management Group-Intervention on Participation in Post-Stroke Patients.

Primary Purpose

Stroke

Status
Terminated
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Self-Management group-intervention
Standard Care
Sponsored by
Uzi Milman
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Self-Management, Stroke, Intervention, Group Processes

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Cerebrovascular accident diagnosed 3-18 months before enrollment. Treated at th Neurologic Rehabilitation Center of Clalit Health Services in Kiryat Byalik, Israel.

Living in the community (in their homes). Are capable of basic communication in Hebrew.

Exclusion Criteria:

Moderate-severe stroke (National Institutes of Health Stroke Scale (NIHSS) score ≤ 16).

Moderate-Severe Cognitive impairment (Montreal Cognitive Assessment (MOCA) - total score ≤ 16). Inability to provide informed consent.

Sites / Locations

  • Clinical Research Unit, Clalit Health Services, Haifa and Western Galilee District,

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Self-Management group-intervention

Standard Care

Arm Description

Participants will receive Self-Management group-intervention + Standard Care

Participants will receive Standard Care only

Outcomes

Primary Outcome Measures

Patient Participation
The primary outcome measure is the change in patient's participation, as defined by the International Classification of Function, Disability and Health (ICF), between the three assessment points - baseline, 12 and 36 weeks.

Secondary Outcome Measures

Self-efficacy for self-management behaviors.
Self-efficacy for self-management behaviors.

Full Information

First Posted
November 10, 2014
Last Updated
September 19, 2019
Sponsor
Uzi Milman
Collaborators
University of Haifa
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1. Study Identification

Unique Protocol Identification Number
NCT02289287
Brief Title
Effects of a Self-Management Group-Intervention on Participation in Post-Stroke Patients.
Official Title
Effects of a Self-Management Group-Intervention on Participation in Post-Stroke Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Terminated
Why Stopped
Due to difficulties in recruitment and academic time constrains we terminated the study after 60 participants instead of 90 as planned.
Study Start Date
April 17, 2017 (Actual)
Primary Completion Date
September 19, 2019 (Actual)
Study Completion Date
September 19, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Uzi Milman
Collaborators
University of Haifa

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Stroke is defined as a sudden vascular accident that causes brain damage and neurological impairment. Literature shows that a stroke has a negative effect on participation. Self-Management (SM) is defined as health promotion and education programs used mostly for people with chronic diseases, which aim at helping patients to maintain a feeling of wellness. The primary aim of this study is to assess the effectiveness of a group-based SM program for post-stroke patients in a community setting, and its contribution to improving participation, compared to standard care.
Detailed Description
At enrollment eligible patients will be randomized to Intervention + Standard Care or Standard Care group. Within 3 weeks after enrollment all participants will undergo baseline assessment using a predefined set of scales and questionnaires (intervention group will additionally undergo a semi-structured interview). The group-intervention (SM program) will begin after enrollment of at least 4 participants to the intervention group, and within no longer than 5 weeks since enrollment. The intervention will include 12 weekly sessions, each session 2.5 hour long, and will be based on well-known SM interventions that were found effective for stroke patients in the U.S. Standard care will include 'one-on-one' sessions in each paramedical discipline as given regularly in this setting (average of 15-20 sessions per patient). Follow-up measures will be performed within a week after the end of the intervention, and 6 months thereafter, in order to examine long term effectiveness. Outcome measures are questionnaires; change will be assessed by the difference in total score between T1 |(pre-intervention), T2 (post-intervention) and T3 (after 6 months)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Self-Management, Stroke, Intervention, Group Processes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Self-Management group-intervention
Arm Type
Experimental
Arm Description
Participants will receive Self-Management group-intervention + Standard Care
Arm Title
Standard Care
Arm Type
Active Comparator
Arm Description
Participants will receive Standard Care only
Intervention Type
Behavioral
Intervention Name(s)
Self-Management group-intervention
Intervention Description
At enrollment eligible patients will be randomized to Intervention + Standard Care or Standard Care group. Within 3 weeks after enrollment all participants will undergo baseline assessment using a predefined set of scales and questionnaires (intervention group will additionally undergo a semi-structured interview). The group-intervention (SM program) will begin after enrollment of at least 4 participants to the intervention group, and within no longer than 5 weeks since enrollment. The intervention will include 12 weekly sessions, each session 2.5 hour long, and will be based on well-known SM interventions that were found effective for stroke patients in the U.S. Follow-up assessments will be done at 12 and 36 week to examine long term effectiveness.
Intervention Type
Behavioral
Intervention Name(s)
Standard Care
Intervention Description
At enrollment eligible patients will be randomized to Intervention + Standard Care or Standard Care group. Within 3 weeks after enrollment all participants will undergo baseline assessment using a predefined set of scales and questionnaires (intervention group will additionally undergo a semi-structured interview). Standard care will include 'one-on-one' sessions in each paramedical discipline as given regularly in this setting (average of 15-20 sessions per patient). Follow-up assessments will be done at 12 and 36 week to examine long term effectiveness.
Primary Outcome Measure Information:
Title
Patient Participation
Description
The primary outcome measure is the change in patient's participation, as defined by the International Classification of Function, Disability and Health (ICF), between the three assessment points - baseline, 12 and 36 weeks.
Time Frame
12 and 36 weeks
Secondary Outcome Measure Information:
Title
Self-efficacy for self-management behaviors.
Description
Self-efficacy for self-management behaviors.
Time Frame
12 and 36 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cerebrovascular accident diagnosed 3-18 months before enrollment. Treated at th Neurologic Rehabilitation Center of Clalit Health Services in Kiryat Byalik, Israel. Living in the community (in their homes). Are capable of basic communication in Hebrew. Exclusion Criteria: Moderate-severe stroke (National Institutes of Health Stroke Scale (NIHSS) score ≤ 16). Moderate-Severe Cognitive impairment (Montreal Cognitive Assessment (MOCA) - total score ≤ 16). Inability to provide informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tamar Adar, MD
Organizational Affiliation
Clinical Research Unit, Clalit Health Services, Haifa District, HAIFA, ISRAEL
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eli Carmeli, PhD
Organizational Affiliation
Department of Physical Therapy, Faculty of Social Well fare and Health Sciences, Haifa University, Haifa, Israel.
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Hagit Harel-Katz, MSc
Organizational Affiliation
Clinical Research Unit, Clalit Health Services, Haifa District, HAIFA, ISRAEL
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Uzi Milman, MD
Organizational Affiliation
Clinical Research Unit, Clalit Health Services, Haifa District, HAIFA, ISRAEL
Official's Role
Study Director
Facility Information:
Facility Name
Clinical Research Unit, Clalit Health Services, Haifa and Western Galilee District,
City
Haifa,
Country
Israel

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32174261
Citation
Harel-Katz H, Adar T, Milman U, Carmeli E. Examining the feasibility and effectiveness of a culturally adapted participation-focused stroke self-management program in a day-rehabilitation setting: A randomized pilot study. Top Stroke Rehabil. 2020 Dec;27(8):577-589. doi: 10.1080/10749357.2020.1738676. Epub 2020 Mar 14.
Results Reference
derived

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Effects of a Self-Management Group-Intervention on Participation in Post-Stroke Patients.

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