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A Feasibility Randomised Controlled Trial of an Online Exercise Programme for Adults With Cerebral Palsy

CP-EXCEL: A Feasibility Randomised Controlled Trial of an Online Exercise Programme for Adults With Cerebral Palsy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06983782
Enrollment
47
Registered
2025-05-21
Start date
2025-07-25
Completion date
2026-03-31
Last updated
2026-08-12

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

Conditions

Adults, Cerebral Palsy, Exercise, Fitness

Keywords

Adults with cerebral palsy, Online exercise programme, physiotherapy

Brief summary

Adults with cerebral palsy (CP) often face challenges in accessing exercise programmes that are appropriate for their needs. Barriers such as limited mobility, a lack of tailored options, and restricted access to physiotherapy services can make participation difficult. Exercise is important for improving physical health, mental well-being, and overall quality of life. However, many adults with CP do not have regular opportunities to take part in structured physical activity. This study aims to investigate whether an online exercise programme can serve as an effective and accessible alternative. The main aim of the study is to assess the feasibility of delivering an online exercise programme for adults with CP. Key areas of focus will include demand, implementation, practicality, adaptability, acceptability, and potential benefits to physical, mental, and social well-being. A total of 60 adults with CP will be recruited and randomly assigned to one of two groups (30 participants per group). One group will complete an 8-week online exercise and education programme. The second group will receive the same educational materials during the study and will be provided with information about the home exercise programme after the 8-week intervention period. Data will be collected on attendance, completion rates, engagement with exercises, and any reported adverse events. Health-related surveys will be completed before and after the programme to assess any changes. In addition, a selected group of participants from the intervention group will take part in interviews to provide feedback on their experiences. Findings from this study may support the development of accessible, effective, and person-centred online exercise programmes for adults with CP. Results may help improve future programme design and contribute to better care and support for adults with CP in Ireland.

Interventions

OTHERExercise and education programme

Participants will complete 8-week online exercise programme consisting of an online exercise class once per week. The exercises will target improving strength, balance and range of movement. In addition, participants will receive educational materials on exercise, nutrition, walking changes, fatigue, optimizing bone health, pain management, mental health, sleep and physical activity maintenance.

OTHERcontrol group

The control group will receive educational materials over 8 weeks

Sponsors

Royal College of Surgeons, Ireland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 and over with cerebral palsy (CP) residing on the island of Ireland. * Individuals of any Gross Motor Function Classification System (GMFCS) level. * Individuals with other associated impairments. * People with mild-to-moderate intellectual disability who can access the online platform and follow study instructions, with or without support.

Exclusion criteria

* Individuals with severe intellectual disability where sufficient adaptations cannot be made. * Adults with unstable medical conditions.

Design outcomes

Primary

MeasureTime frameDescription
Physical functionDuration of study 2 yearsPhysical function will be measured using the PROMIS physical function- Short Form 10a scale.
Mobilityrolling recruitment over 1.2 yearsMobility will be measured using the Functional mobility scale on a scale of 0-6.
Presence of PainDuration of study 2 yearsPain will be assessed using a self-reported questionnaire, measured as Yes or No with description.

Secondary

MeasureTime frameDescription
Pain intensityDuration of study 2 yearsPain intensity will be measured using the PROMIS Pain intensity form
Pain qualityDuration of study 2 yearsPain quality will be assessed using the PROMIS Neuropathic Pain Quality 5a and Nociceptive Pain Quality 5a scales, with total scores calculated for each to reflect the severity and type of pain experienced.
Pain interferenceDuration of study 2 yearsPain quality will be assessed using the PROMIS Pain interference Short Form-8a, with total scores calculated to reflect the quality of pain experienced.
FatigueDuration of study 2 yearsFatigue will be assessed using the PROMIS Fatigue Short Form 13a (FACIT Fatigue) scale, with total scores calculated to reflect the severity of fatigue experienced by participants.
SleepDuration of study 2 yearsSleep will be assessed using the PROMIS Sleep Disturbance Short Form 4a scale, with total scores reflecting the extent of sleep disturbance experienced by participants.
Self-efficacyDuration of study 2 yearsSelf-efficacy will be assessed using two PROMIS Short Form scales: the Self-Efficacy for Managing Chronic Conditions - Managing Daily Activities (Short Form 8a) and the Self-Efficacy for Managing Chronic Conditions - Managing Emotions. Total scores from each scale will reflect participants' confidence in managing daily activities and emotional responses related to their condition.
DepressionDuration of study 2 yearsDepression will be assessed using the PROMIS Emotional Distress - Depression Short Form 8a, with total scores reflecting the severity of depressive symptoms experienced by participants.
ParticipationDuration of study 2 yearsParticipation will be assessed using the PROMIS Ability to Participate in Social Roles and Activities Short Form 8a, with total scores indicating the extent to which participants are able to engage in social roles and daily activities.

Countries

Ireland

Contacts

PRINCIPAL_INVESTIGATORJennifer M Ryan, PhD

Royal College of Surgeons in Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026