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The Introduction of Petra Running-bikes: A Pilot Study

The introduction of Petra running-bikes to encourage and facilitate weight-bearing exercise for children with cerebral palsy who are unable to walk independently: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN37572029
Enrollment
12
Registered
2013-12-17
Start date
2013-08-19
Completion date
Unknown
Last updated
2017-02-20

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

Conditions

Topic: Generic Health Relevance and Cross Cutting Themes

Interventions

A minimum of 12 children aged 4-12 years will be recruited for this pilot study. This will provide sufficient data to answer the research question "can non-ambulant children with cerebral palsy use an

Sponsors

Sussex Community NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Children with CP aged 4 to 12 years 2. Children with CP who are unable to walk independently (Gross Motor Function Classification levels III, IV or V) 3. Ability to follow instructions to use the running-bikes 4. Target Gender: Male & Female

Exclusion criteria

Exclusion criteria: 1. Children under the age of 4, or over the age of 12 years. 2. Children with CP who are able to walk (Gross Motor Function Classification Levels I or II) 3. Children who have undergone orthopaedic surgery to the spine or lower limbs within the last six months (due to the risk of fracture). 4. Children with a history of leg fractures (who may be vulnerable to further fracture). 5. Children with cognitive or behavioural impairment (preventing simple instructions on how to manoevre the running-bike). 6. Children with serious visual impairment (safety issues regarding using the runningbike).

Design outcomes

Primary

MeasureTime frame
Ability to use the running bike; Timepoint(s): This will be assessed and scored on 3 occassions (baseline, week 6 and week 12).

Secondary

MeasureTime frame
1. Bone health; Timepoint(s): Bone status will be assessed using an ultrasound bone densitometer at baseline and week 12 2. Focus group feedback from participants; Timepoint(s): Week 13 3. Gross Motor Function; Timepoint(s): Standing ability will be assessed at baseline and week 12 4. Quality of life; Timepoint(s): QoL will be assessed at baseline and week 12.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026