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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON55033

Enrollment

Registered

2020-07-01

Start date

2021-03-02

Completion date

Unknown

Last updated

2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovasculair, beroerte Sedendary behavriour after stroke sitting time after stroke

Interventions

Participants will receive the RISE intervention, a blended movement behaviour change intervention that aims to support them to reduce and interrupt their sedentary time. The blended intervention is

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria: 1. Insufficient knowledge of the Dutch language to understand the intervention content; 2. Score

Design outcomes

Primary

Measure	Time frame
1. Preliminary effectiveness of the intervention on sedentary behaviour; total amount of sedentary time and the sedentary time fragmentation. 2. Feasibility of the intervention; compliance, satisfaction and safety.	—

Secondary

Measure	Time frame
Secondary study outcome: 1. Preliminary effectiveness of the intervention with PS on sedentary behaviour; total amount of sedentary time and the sedentary time fragmentation 2. Feasibility of the intervention with PS; compliance and safety 3. Preliminary effectiveness of the intervention on non-sedentary movement behaviour; the amount of light and moderate to vigorous physical activity, the step count and the time spent standing and/or walking. Other study parameters: participant characteristics, sleep duration and quality, happiness, tiredness, stress, pain, time pressure, the inclusion rate, time consumption of the intervention and the study and the activity monitor data and the usage of the different parts of the app during the intervention.	—

Measure

Time frame

Secondary study outcome: 1. Preliminary effectiveness of the intervention with PS on sedentary behaviour; total amount of sedentary time and the sedentary time fragmentation 2. Feasibility of the intervention with PS; compliance and safety 3. Preliminary effectiveness of the intervention on non-sedentary movement behaviour; the amount of light and moderate to vigorous physical activity, the step count and the time spent standing and/or walking. Other study parameters: participant characteristics, sleep duration and quality, happiness, tiredness, stress, pain, time pressure, the inclusion rate, time consumption of the intervention and the study and the activity monitor data and the usage of the different parts of the app during the intervention.

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Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026