Vitality: Promoting Cognitive Function in Older Adults With Chronic Stroke

NCT01916486 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2020-08-28

No results posted yet for this study

Summary

The investigators will conduct a randomized controlled trial study to provide preliminary evidence of efficacy of exercise training or a complex mental and social activities program for improving cognitive function in older adults with chronic stroke, compared with a stretch and relaxation program.

Conditions

Interventions

BEHAVIORAL

Exercise training

The EX Program will provide objective progression in the guided exercises of each participant.

BEHAVIORAL

Complex mental and social activities

The Cog-Plus Program will engage participants in activities promoting cognitive function and socialization.

BEHAVIORAL

Control: stretching and relaxation program

The CON Program consist of stretches, deep breathing and relaxation techniques, general posture education, and general core control exercises in the sitting position.

Sponsors & Collaborators

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • University of British Columbia

    lead OTHER

Principal Investigators

  • Janice J Eng, PhD, PT · University of British Columbia

  • Teresa Liu-Ambrose, PhD, PT · University of British Columbia

  • Peter Hall, PhD · University of Waterloo

  • Charlie Goldsmith, PhD · Simon Fraser University

  • Jennifer Davis, PhD · University of British Columbia

  • Laura Middleton, PhD · University of Waterloo

  • Ging-Yuek Robin Hsiung, MD · University of British Columbia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2019-08-31
Completion
2020-02-29

Countries

  • Canada

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01916486 on ClinicalTrials.gov