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Feasibility Randomised-Controlled Trial of Online Stroke Interventions

NCT05461937 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2024-05-29

No results posted yet for this study

Summary

Many people have difficulties organising their behaviour and problem-solving (also known as executive function difficulties) after stroke. This can have serious, wide-ranging consequences for wellbeing and ability to regain independence. Currently, access to psychological interventions after stroke varies and there is not enough evidence to recommend a specific intervention for executive function difficulties after stroke. A short intervention was designed to help with executive function difficulties by making it easier to set goals and achieve them after stroke. The intervention is designed for online delivery to make it accessible to as many stroke survivors as possible. The present trial aims to investigate the acceptability and feasibility of a single blinded randomized controlled trial of this online executive function intervention (active intervention) compared to an online stroke psychoeducation intervention (control intervention).

Conditions

Interventions

BEHAVIORAL

Getting things done after stroke

A two-session, online rehabilitation intervention focussing on cognitive executive functions supplemented with weekly homework tasks.

BEHAVIORAL

Stroke psychoeducation

A two-session, online stroke psycho-education intervention supplemented with weekly homework tasks.

Sponsors & Collaborators

  • University of East Anglia

    lead OTHER

Principal Investigators

  • Catherine EL Ford, PhD · University of East Anglia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-10
Primary Completion
2023-09-15
Completion
2023-09-15

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05461937 on ClinicalTrials.gov