Recruiting NA Stroke

New treatment option for Stroke

Official title The Active Transition Home Post-Stroke Program

ClinicalTrials.gov ID: NCT06119230

What this study is testing

What it's testing
Post-stroke participants will wear wearable sensors for one week at 1-week prior to discharge from inpatient rehabilitation, 3- and 7- weeks post-discharge and 3-months post-discharge. All participants will wear sensors but only participants in the intervention group will receive sensor-informed activity feedback (e.g., activity, sleep and sedentary behaviour) and feedback informed goal setting sessions with a physiotherapist.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Physiotherapists for focus group participation
  • Age of 18 or older
  • Registered Physiotherapist at GF Strong (inpatient or outpatient)
  • 1 year of work experience in stroke rehabilitation (acute or chronic) Patient Group
  • Age of 18 or older

You likely can't join if

  • Physiotherapist Focus Group:
  • \- \<1 year of experience in stroke rehabilitation
  • Patient Group:
  • \- presents with any other unstable medical conditions that would impact activity (e.g., unstable cardiac condition, recent fracture)
See the full eligibility criteria
Who can join
  • Physiotherapists for focus group participation
  • Age of 18 or older
  • Registered Physiotherapist at GF Strong (inpatient or outpatient)
  • 1 year of work experience in stroke rehabilitation (acute or chronic) Patient Group
  • Age of 18 or older
  • Had a stroke resulting in hemiparesis
  • English speaking or living with an English-speaking family member to assist with interpretation/goal setting with PT
What rules you out
  • Physiotherapist Focus Group:
  • \- \<1 year of experience in stroke rehabilitation
  • Patient Group:
  • \- presents with any other unstable medical conditions that would impact activity (e.g., unstable cardiac condition, recent fracture)

The study team makes the final eligibility decision.

Where it's taking place

  • Vancouver, British Columbia, Canada

Compensation & support

Compensation mentioned.

ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.

Questions & answers

Do participants get paid in this trial?

This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Vancouver, British Columbia, Canada. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.