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MONitoring Sedentary Behavior and Light Physical Activity in Patients With Stroke (MONSS)

Z

Zealand University Hospital

Status

Enrolling

Conditions

Behavior
Physical Inactivity
Stroke, Acute
Sedentary Behavior

Treatments

Behavioral: Everyday Life is Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

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.

Enrollment

100 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Verified ischemic stroke or intracerebral hemorrhage
  • Modified rankin score (mRS) 1-3 at discharge
  • Discharged with at rehabilitation plan within 1-14 hospitalization days
  • Able to ambulate independently
  • Speak and understand Danish

Exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

100 participants in 2 patient groups

Intervention
Experimental group
Treatment:
Behavioral: Everyday Life is Rehabilitation
Control
No Intervention group

Trial contacts and locations

1

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Central trial contact

Stefan S Bodilsen, MSPT

Data sourced from clinicaltrials.gov

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