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The Whole Day Matters After Stroke (BIG-STEPS)

Stroke

Goal of research program: To understand person-specific factors, such as imaging markers and activity patterns early after stroke, that may guide precision rehabilitation to optimize function and improve recovery.

Objectives:

1. Test the effect of reducing sedentary behaviour early after stroke on functional mobility and global disability outcomes.
2. Determine the impact of neuroimaging biomarkers (e.g. leukoaraiosis) on response to rehabilitation.
3. Explore the predictive value of accelerometry as an adjunct to the subjective modified Rankin Scale (mRS) to assess functional disability after stroke.

Experimental approach/Research Plan/Use of Funds: The investigators aim to recruit 50 participants within 1 week of ischemic stroke onset, aged ≥ 18 years, medically stable as deemed by their physicians, able to walk at least 5 meters with/without gait aid and with ongoing walking or balance goals. Demographic and stroke characteristics, including stroke risk factors, infarct location and volume, leukoaraiosis on routine MRI, and acute stroke treatments (e.g., thrombectomy) will be determined and documented. A battery of impairment, psychosocial, and functional measures, including the mRS and Timed-Up and Go test (primary outcomes) will be completed. Subsequently, participants will be set up to wear activPAL accelerometer, validated in stroke, for 1 week. Following randomization, a sedentary behaviour change intervention will span 6 weeks, with final follow-up assessments at 90 days.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Within 7 days of ischemic stroke onset
* Aged ≥ 18 years
* Medically stable as deemed by physicians
* Able to walk at least 5 meters with/without gait aid
* Ongoing walking goals (walk speed \<1.0 meter/sec)

Exclusion Criteria:

* Have another condition such as multiple sclerosis or Parkinson's disease, or active cancer
* Uncontrolled high blood pressure
* Unstable cardiovascular condition
* Unable to understand or follow instructions.

Study Location

University of Alberta Hospital
University of Alberta Hospital
Edmonton, Alberta
Canada

Contact Study Team

Primary Contact

Victor Ezeugwu, PT, PhD

[email protected]
7804925108
Study Sponsored By
University of Alberta
Participants Required
More Information
Study ID: NCT05753761