NCT06409351

Multi-modal Training Program to Promote Physical Activity After Stroke: A Randomised Controlled Trial.

Multi-mOdal Training Program to Promote Physical actIVity After sTrokE: MOTIVATE - a Hybrid Type 1 Randomized Controlled Trial
Singapore General Hospital·ClinicalTrials.gov·behavioralNot yet recruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Intervention group
Study type
Interventional
Intervention type
behavioral
Sponsor & location
Primary sponsor
Singapore General Hospital
Location
Singapore, Singapore
Timeline & enrollment
Phase
N/A
Start date
May 01, 2024
End date
Mar 31, 2026
Enrollment
120 participants
Primary outcome

Duration of moderate to vigorous physical activity

Summary

The goal of this study is to learn if a behavioral change intervention can improve physical
 activity in stroke survivors living in the community.
 
 The main question it aims to answer is, if a behaviour change intervention and personalised
 physical activity prescription, are effective in improving the time spent in moderate to
 vigorous physical activity amongst chronic stroke survivors.
 
 Researchers will compare the intervention group to a control group, to see if physical
 activity counselling and a personalized physical activity prescription is more effective in
 improving moderate to vigorous physical activity, than usual care alone. The study period for
 each participant is 6 months. Assessments are conducted at month 1 (baseline), 3 and 6.
 
 The control group will receive only usual care, which consists of an information sheet on
 physical activity with the following content: (1) Why be active and (2) How to be active
 (with URL links to resources and videos). The usual care is delivered at 3-time points during
 month 1, 3 and 6.
 
 The intervention group will receive usual care and a behavioral change intervention. The
 behavioral change intervention consists of up to 6 individual physical activity counselling
 sessions and a personalized physical activity prescription. The 6 sessions will take place
 only during months 1 to 3 and there will be no intervention during months 4 to 6. Of the 6
 sessions, 3 are conducted face-to-face and another 3 sessions will take place using
 telehealth methods such as phone, text messaging and videoconference. Participants can meet
 the study physiotherapist at their preferred exercise space during the 3 face-to-face
 sessions. The physical activity counselling sessions consist of goal setting and action
 planning, and problem-solving barriers around participation in physical activity. The overall
 aim is to increase time spent in moderate-vigorous physical activity.

ICD-10 classifications
Stroke, not specified as haemorrhage or infarctionSequelae of stroke, not specified as haemorrhage or infarctionCerebral infarctionCerebral infarction, unspecifiedAcquired absence of hand and wrist
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06409351
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06409351 through Pure Global AI's free database. This phase not specified trial is sponsored by Singapore General Hospital and is currently Not yet recruiting. The study focuses on Stroke,Physical Inactivity. Target enrollment is 120 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.