Increasing Physical Activity in Stroke Survivors Using STARFISH, an Interactive Mobile Phone App

NCT02494245 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2017-06-01

No results posted yet for this study

Summary

The aim of the study is to compare physical activity in stroke survivors who have undertaken a four month physical activity intervention using the STARFISH application with a control group receiving four months of usual care.

Conditions

Interventions

OTHER

STARFISH

The intervention group will take part in a four month physical activity intervention using the STARFISH app with the aim of increasing physical activity by 3000 steps per day. Participants will be provided with a smartphone for the intervention. Participants will work in groups of four but each participant will have their own individualised step count target, based on their baseline step count. If the participant reaches their step count target on at least five days of the week, then their target will be increased by 5% for the following week, up to a maximum increase of 3000 steps above baseline. Where a participant fails to reach their step count target, it remains unchanged for the following week.

Sponsors & Collaborators

  • Chest, Heart and Stroke Association Scotland

    collaborator OTHER
  • NHS Greater Glasgow and Clyde

    collaborator OTHER
  • National Heatlh Service Ayrshire and Arran

    collaborator OTHER_GOV
  • National Health Service Lanarkshire

    collaborator UNKNOWN
  • University of Glasgow

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-31
Primary Completion
2017-10-31
Completion
2017-10-31

Countries

  • United Kingdom

Study Locations

More Related Trials

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 NCT02494245 on ClinicalTrials.gov