Actively Recruiting

Phase Not Applicable
All Genders
NCT05793177

MONitoring Sedentary Behavior and Light Physical Activity in Patients With Stroke

Led by Zealand University Hospital · Updated on 2024-07-25

100

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized control trial (RCT) aims to test the effect of a 12 weeks tailored behavioral intervention on stroke survivors living in the community and compare the results to a control group of stroke survivors participating in standard care. The intervention's purpose is to lower the time spend with sedentary behavior and raise the level of physical activity in stroke survivors throughout their everyday life. The intervention contains two motivational interviews with a focus on goal setting, action planning, motivation, fatigue management, and general information on life after stroke. The primary outcome for behavior change is objectively measured physical activity using an activity tracker (ActivPal4 Micro) and secondary glycohemoglobin and changes in quality of life.

CONDITIONS

Official Title

MONitoring Sedentary Behavior and Light Physical Activity in Patients With Stroke

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Verified ischemic stroke or intracerebral hemorrhage
  • Modified Rankin score (mRS) 1-3 at discharge
  • Discharged with a rehabilitation plan within 1-14 days of hospitalization
  • Able to ambulate independently
  • Speak and understand Danish
Not Eligible

You will not qualify if you...

  • Aphasia
  • Unable to give informed consent
  • Unable to ambulate independently
  • Mental illness
  • Other co-morbidity such as terminal cancer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Zealand University hospital

Roskilde, Denmark, 4000

Actively Recruiting

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Research Team

S

Stefan S Bodilsen, MSPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

2

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