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Feasibility study of the ExTraChild-project

Feasibility study of exercise training among children with cerebral palsy to increase health and wellbeing (ExTraChild-project a sub-study of the LEER-project

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14737272
Enrollment
8
Registered
2025-06-09
Start date
2024-03-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Exercise training among children with cerebral palsy to increase health and well-being Nervous System Diseases

Interventions

Two different exercise regimes on spinning-bikes, Moderate Intensity Continuous Training (MICT) and High Intensity Interval Training (HIIT), will be performed three times per week for 16-weeks with 16
lifestyle changes as well as interventions must be implemented through the family. Feasibility testing aims to analyze clinical, procedural, and methodological uncertainties of the exercise testing an

Sponsors

Lund University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Ambulant children with CP defined as GMFCS-E&R I-II 2. Healthy controls: ambulant children who are TD and not participating in any regular and planned leisure time physical exercise will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Ambulant children with CP walking with a walking aid (GMFCS-E&R III) 2. Ambulant children who are TD with other neurological diagnoses, metabolic diagnoses, orthopaedic disabilities, asthma, heart diseases, cognitive impairment, or indigestion of regular medication.

Design outcomes

Primary

MeasureTime frame
Number of completed exercise sessions measured using patient records at end of study

Secondary

MeasureTime frame
1. Number of completed tests measured using patient records at end of study 2. Exercise test VO2, VCO2, VE, RER, BF, VO2/kg adn HR before and after exercise period. 3. Body composition by bio impedance before and after exercise period. 4. Range of motion according to CPUP before and after exercise period. 5. Spaticity according to CPUP before and after exercise period. 6. Variance i watt during each exercise session. 7. Variance in HR during each exercise session. 8. Physical activity assessed by accelerometry before and after exercise period. 9. Quality of life (EQ5D) before and after exercise period. 10. Bowl function assessed by the Bristol scale before and after exercise period. 11. Changes in blood biomarkers BDNF, VEGF, ACTH, GH, CRP, IL-6, IGF-1, IGFBP-3, TNF-a and insulin, assessed in plasma collected from venues blood sampling before and after each exercise test performed before and after the exercise period 12. Capillary blood glucose and lactate collected before and after each exercise test performed before and after the exercise period. 13. Semi-structed interviews about the experiences of participating in the testing and exercise sessions

Countries

Sweden

Contacts

Public ContactÅsa Tornberg
asa.tornberg@med.lu.se+46-46-222 97 64

Outcome results

None listed

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