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PARAS: A feasibility study of an intervention targeting Physical Activity Routines After Stroke

A feasibility, acceptability and fidelity study of a multifaceted behaviour change intervention targeting free-living physical activity and sedentary behaviour after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN35516780
Enrollment
57
Registered
2018-10-24
Start date
2018-10-03
Completion date
Unknown
Last updated
2022-11-14

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

Conditions

Physical activity in people who have had a stroke Nervous System Diseases Stroke

Interventions

At the baseline, the following socio-demographic and health information measures will be collected from the stroke survivors: age (years), sex (male/female), pre-morbid walking status (independent/wal
date of stroke
assistive device use (no device/stick/tripod/elbow crutches/zimmer frame/delta frame/four wheeled walker/wheelchair/other). The following will also be completed: Rivermead Mobility Index, Fatigue Asse

Sponsors

Northumbria Healthcare NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Stroke survivors: 1. Adult community dwelling stroke survivors 2. Currently receiving outpatient/community stroke rehabilitation in the study catchment area 3. Capacity to provide informed consent 4. Capability to undertake a supported self-management physical activity intervention programme (e.g. not requiring high levels of hands on therapy for function) 5. Agreement by the therapist and patient that there is capacity for increased activity/less sedentary behaviour Healthcare professionals: 1. Currently working as a healthcare professional (e.g. physiotherapists, occupational therapists and rehabilitation assistants) delivering home/community based stroke rehabilitation 2. Capacity and willingness to undertake intervention training, delivery and assessment throughout study duration 3. Ability to deliver the intervention programme to up to five stroke survivors

Exclusion criteria

Exclusion criteria: Stroke survivors: 1. Contraindications for undertaking physical activity e.g. presence of unstable heart disease 2. Advised by GP/Consultant not to undertake physical activity for health reasons

Design outcomes

Primary

MeasureTime frame
The overall aim of this study is to assess the feasibility, acceptability and fidelity of a theory- and evidence-based multifaceted behaviour change intervention targeting free-living physical activity and sedentary behaviour after stroke. In order to assess the feasibility, acceptability and fidelity of the intervention the following outcomes will be collected at the baseline and at the review: 1. Stroke survivor and healthcare professional study recruitment and attrition rates, calculated as rate per month 2. Feasibility of intervention delivery, described using: 2.1. The number of and time taken (minutes) for face-to-face/telephone intervention delivery 2.2. The application of the different intervention components applied (e.g. self-monitoring tools, activity selection) 2.3. Safety reporting 3. Completeness of baseline and review descriptive data to determine the feasibility of the inclusion criteria and of potential outcome measures. Baseline demographics will be collected and at baseline and reviews (the timing of the reviews is individualised to the participant) the following measures will be made: 3.1. Warwick-Edinburgh Mental Well-Being Scale 3.2. Fatigue Assessment Scale 3.3. Rivermead Mobility Assessment 4. Views of stroke survivors and healthcare professionals on the acceptability of the intervention and study protocol, assessed using a questionnaire and interview 5. Fidelity of delivery, receipt and enactment of the intervention, assessed through analysis of audio recordings of healthcare profressional delivered sessions and intervention documentation

Countries

England, United Kingdom

Contacts

Public ContactSarah Moore
s.a.moore@ncl.ac.uk+44 (0)1912083837

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 27, 2026