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Home-based E-biking Intervention Among Individuals With Cerebral Palsy

Research Protocol for Feasibility Testing of 12 Weeks Home-based E-biking Intervention Among Individuals With Cerebral Palsy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06402799
Enrollment
23
Registered
2024-05-07
Start date
2023-11-01
Completion date
2024-05-18
Last updated
2024-10-04

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

Conditions

Cerebral Palsy

Keywords

Home-based, e-biking, monitoring, cerebral palsy, feasibility

Brief summary

Investigation of the feasibility of virtually group-based e-biking training at home. Individuals aged 13-60 years with CP (Cerebral Palsy) with a Gross Motor Function Classification System score of 1-3 were recruited for a 12-week home-based e-biking training program.

Detailed description

All participants should be able to use a touchscreen, as this type of technology is used in the virtual e-biking training. Participants complete a questionnaire and subsequently engage in 12 weeks of home-based virtual e-biking training. A loaned bicycle will be provided for the training period and set up in the participants' own homes. Setup and adjustments will be performed by trained healthcare personnel. The following measurements will be taken before and after the training period: weight, height, hip-waist measurements, blood pressure, a 30-second sit-to-stand test, a timed-up-and-go test, ankle measurements, and a functional threshold power test (FTP). Seven accelerometers will be attached to the right and left arms, thighs, lower legs, and sternum using NJaP patches and worn for 72 hours at the beginning and end of the training period. The accelerometers can be easily removed after 72 hours. The e-biking intervention consists of 3 sessions per week at the beginning of the study and gradually increases over the training period to 6 sessions per week, with three of these sessions being online and group-supervised.

Interventions

BEHAVIORALHome-based E-biking

The e-biking intervention consists of 3 sessions per week at the beginning of the study and gradually increases over the training period to 6 sessions per week, with three of these sessions being online and group-supervised. Heart rate will be monitored as well as power in Watt at each session.

Sponsors

University of Copenhagen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Feasibility of home-based e-biking among individuals with cerebral palsy. The e-biking intervention consists of 3 sessions per week at the beginning of the study and gradually increases over the training period to 6 sessions per week, with three of these sessions being online and group-supervised.

Eligibility

Sex/Gender
ALL
Age
13 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Individuals with cerebral palsy (GMFCS 1-3) * Are able to keep balance on a stationary bike * Are able to use a touchscreen

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of study assessed by minimum 70% participation in planned training volume among participantsAt the end of the study (after 12 weeks of e-biking training)Number of participants who complete the study successfully assessed by percentage of completed planned training volume

Secondary

MeasureTime frameDescription
Change in FTP test among participantsAt the end of the study (after 12 weeks of e-biking training)The functional threshold power test will change after the intervention as the participants achieve better fitness
Change in timed-up-and-go testAt the end of the study (after 12 weeks of e-biking training)The timed-up-an-go test will change after the intervention
Change in the 30-seconds sit-to-stand testAt the end of the study (after 12 weeks of e-biking training)The 30-seconds sit-to-stand test will change after the intervention

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026