Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05511285

Improving Sleep and Learning in Rehabilitation After Stroke, Part 2

Led by University of Oxford · Updated on 2025-11-18

100

Participants Needed

1

Research Sites

193 weeks

Total Duration

On this page

Sponsors

U

University of Oxford

Lead Sponsor

B

Big Health Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will explore whether sleep in stroke survivors is improved with digital cognitive behavioural therapy for insomnia (Sleepio), in comparison to treatment as usual, and will explore whether changes in sleep relate to changes in overnight consolidation of motor learning.

CONDITIONS

Official Title

Improving Sleep and Learning in Rehabilitation After Stroke, Part 2

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing and able to give informed consent for participation in the study
  • Aged 18 years or above
  • Clinical diagnosis of stroke affecting the upper limb, with sufficient movement to perform the motor learning task
  • Discharged from inpatient care
  • Interest in accessing a programme with the aim of improving sleep quality
  • Reliable access to the internet
Not Eligible

You will not qualify if you...

  • Other neurological condition affecting movement (e.g. Parkinson's Disease, Multiple Sclerosis)
  • Diagnosed, untreated, sleep disorder (e.g. Sleep Apnea)
  • Uncontrolled seizures
  • Planned inpatient admission (e.g. for rehabilitation) in the next 4 months that would impact ability to engage with the Sleepio programme
  • Engagement in psychological therapy for insomnia in the past 12 months
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Oxford

Oxford, United Kingdom, OX39DU

Actively Recruiting

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Research Team

M

Melanie K Fleming, Dr

CONTACT

B

Barbara Robinson

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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