Preliminary effectiveness and feasibility of the RISE intervention to reduce and interrupt sedentary behaviour in community dwelling sedentary people after stroke.

Completed

• Conditions: Cardiovasculair, beroerte; Sedendary behavriour after stroke; sitting time after stroke; 10024450

• Registration Number: NL-OMON55033
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 12

Inclusion Criteria

1. Aged 18 years or older;
2. Stroke diagnosed in hospital within six months of the start of the RISE
intervention;
3. Able to walk independently, as defined by a Functional ambulation categories
score of at least 3;
4. Sedentary prolonger; i.e. *9.5 hours of sedentary time per day and meeting
at least one of the following criteria: >50% of the sedentary time is spent in
bouts > 30 minutes and not reaching the physical activity guideline (150
minutes MVPA during the week);
5. Independent regarding activities of daily living pre-stroke, as defined by a
Barthel Index score of >18;
6. Discharged to the home-setting;
7. Have someone who can participate as a bubby in the RISE intervention with
PS;
8. Given their written informed consent.

Exclusion Criteria

1. Insufficient knowledge of the Dutch language to understand the intervention
content;
2. Score <4 on the Utrecht Communication Assessment (UCO) to understand
questionnaires and follow instructions;
3. Severe comorbidities that prevent that person from safely reducing and
interrupting their sedentary time (e.g. sever pulmonary diseases, hart failure
or malignity*s) as determined with the Physical Activity Readiness
Questionnaire (PAR-Q);
4. Not receiving physiotherapy in any other setting then primary care.

Study & Design

• Study Type: Interventional
• Study Design: Not specified