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Sit-to-Stand Training for Survivors of Stroke in a Long-Term Care Setting

Primary Purpose

Cerebrovascular Accident

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Sit-To-Stand Protocol and Extra Practice in Sit-To-Stand
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebrovascular Accident focused on measuring Long-Term Care, Clinical Protocols, Sit-To-Stand

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of cerebrovascular accident Reside in Long-Term Care Facility Have physician approval to participate in the study Are unable to stand up independently from a 16" surface without using their hands Have given informed consent Exclusion Criteria: Expect to be leaving the facility in less than 24 weeks Have a terminal illness Have a total hip replacement or other orthopedic complication that prevents them from being able to safely use protocol Have pain that prevents their participation Are at higher risk for falling (i.e. blood pressure disorder/postural hypotension, vestibular disorder)

Sites / Locations

  • Hamilton Health Sciences, Chedoke Site

Outcomes

Primary Outcome Measures

Ability to independently perform Sit-To-Stand at 12 weeks and 24 weeks
Score on quality of life measure (COOP) at 12 and 24 weeks
Score on stroke assessment (CMSA) at 12 and 24 weeks

Secondary Outcome Measures

Number of resident falls at 12 and 24 weeks
Number of staff injuries at 12 and 24 weeks
Knowledge of staff on STS protocol immediately post-training, 12 and 24 weeks
Score on quality of life measure (SF-20) at 12 and 24 weeks

Full Information

First Posted
September 13, 2005
Last Updated
September 13, 2005
Sponsor
Hamilton Health Sciences Corporation
Collaborators
Ontario Ministry of Health and Long Term Care
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1. Study Identification

Unique Protocol Identification Number
NCT00197509
Brief Title
Sit-to-Stand Training for Survivors of Stroke in a Long-Term Care Setting
Official Title
Task Specific Training for Stroke Patients
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Unknown status
Study Start Date
January 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Hamilton Health Sciences Corporation
Collaborators
Ontario Ministry of Health and Long Term Care

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to see if providing training using a Sit-to-Stand protocol for residents of Long-Term Care Facilities who have had a stroke will increase their independence in performing Sit-to-Stand.
Detailed Description
The implementation of a sit-to-stand protocol and extra practice has been previously validated in a rehabilitation setting, where 68% of survivors of stroke who received the training, learned to stand safely and independently from a 16" surface (the height of a regular toilet). Our findings have been supported by other research that have shown that rising from sitting is a maneuver that has been advocated for strengthening the lower extremities of elderly individuals and patients with specific disorders such as stroke. During the acute care and rehabilitation phases, considerable effort is spent to maximize a person's functional abilities following a stroke; however, continued strengthening and activity appears to stop once an individual is admitted to a LTC facility. The main purpose of this randomized controlled trial is to examine the efficacy of implementing the Sit-to-Stand (STS) protocol with or without extra sit-to-stand practice for survivors of stroke residing in Long-Term Care (LTC) facilities on (1) their ability to learn how to stand safely and independently from a 16" surface; (2) the number of staff injuries; (3) the number of residents' falls; (4) the quality of life of the residents and staff; and (5) the translation and maintenance of knowledge of the STS protocol by staff into their daily routines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebrovascular Accident
Keywords
Long-Term Care, Clinical Protocols, Sit-To-Stand

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Sit-To-Stand Protocol and Extra Practice in Sit-To-Stand
Primary Outcome Measure Information:
Title
Ability to independently perform Sit-To-Stand at 12 weeks and 24 weeks
Title
Score on quality of life measure (COOP) at 12 and 24 weeks
Title
Score on stroke assessment (CMSA) at 12 and 24 weeks
Secondary Outcome Measure Information:
Title
Number of resident falls at 12 and 24 weeks
Title
Number of staff injuries at 12 and 24 weeks
Title
Knowledge of staff on STS protocol immediately post-training, 12 and 24 weeks
Title
Score on quality of life measure (SF-20) at 12 and 24 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of cerebrovascular accident Reside in Long-Term Care Facility Have physician approval to participate in the study Are unable to stand up independently from a 16" surface without using their hands Have given informed consent Exclusion Criteria: Expect to be leaving the facility in less than 24 weeks Have a terminal illness Have a total hip replacement or other orthopedic complication that prevents them from being able to safely use protocol Have pain that prevents their participation Are at higher risk for falling (i.e. blood pressure disorder/postural hypotension, vestibular disorder)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan R Barreca, PT, BA
Organizational Affiliation
Hamilton Health Sciences Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamilton Health Sciences, Chedoke Site
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 3Z5
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Sit-to-Stand Training for Survivors of Stroke in a Long-Term Care Setting

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