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

H

Hamilton Health Sciences (HHS)

Status and phase

Unknown
Phase 2

Conditions

Cerebrovascular Accident

Treatments

Behavioral: Sit-To-Stand Protocol and Extra Practice in Sit-To-Stand

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Sex

All

Volunteers

No 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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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