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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03668548
Other study ID # REC.18.85.7
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date August 20, 2018
Est. completion date October 22, 2018

Study information

Verified date August 2018
Source St Mary's University College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the effects of 10-weeks leucine supplementation on muscle growth, metabolism, body composition, inflammation and wellbeing in adolescents and young adults with CP.


Description:

Cerebral palsy (CP) is caused by damage to the developing brain and descending pathways, leading to altered patterns of growth and development. Those with CP may encounter early symptoms of paresis and spasticity, leading to progressive secondary musculoskeletal complications, including increased muscle atrophy and abnormal growth of contractile and non‐contractile tissue. This causes significant weakness of the muscle and compromises daily motor function, leading to substantial declines in activities of daily living and independence. As such, interventions aimed at increasing muscle mass or preventing muscle atrophy for those with CP must be established. It is well established that dietary protein ingestion stimulates protein synthesis and inhibits proteolytic pathways, resulting in a positive protein balance and net muscle mass gain. In particular, leucine (a branched chain amino acid; BCAA), has been used to facilitate protein synthesis and muscle growth. Leucine also has anti-inflammatory roles, some of which are central in origin and have been shown to effect mood and features of wellbeing. However, there has been no investigation of the effects of leucine supplementation on any of these parameters in CP. Therefore, the purpose of this study is to assess the effects of 10-weeks leucine supplementation on muscle growth, metabolism, body composition, inflammation and wellbeing in adolescents and young adults with CP.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 25
Est. completion date October 22, 2018
Est. primary completion date October 22, 2018
Accepts healthy volunteers No
Gender All
Age group 12 Years to 40 Years
Eligibility Inclusion Criteria:

- A diagnosis of spastic cerebral palsy

- Aged 12-22 years

Exclusion Criteria:

- Orthopaedic surgery of the upper-limbs in the past 12 months

- Botulinum toxin type A injections in the past 6 months

- Serial casting in the past 6 months

- Insufficient cognitive understanding to comply with the assessment procedures and intervention

- Liver and/or kidney dysfunction

Study Design


Intervention

Dietary Supplement:
Leucine
192 mg/kg body mass/day
Placebo
A taste and calorie-matched placebo

Locations

Country Name City State
United Kingdom University of Gloucestershire Cheltenham Gloucestershire
United Kingdom St Marys Umiversity College London

Sponsors (2)

Lead Sponsor Collaborator
St Mary's University College University of Gloucestershire

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skeletal muscle volume Change in biceps brachii volume 10 weeks
Secondary Resting metabolic rate Change in resting energy expenditure and substrate metabolism 10 weeks
Secondary Perceptual well-being questionnaire Change in a composite measure of five different wellbeing sub-components 10 weeks
Secondary Systemic inflammation (C-Reactive protein; C-RP) Change in C-RP 10 weeks
Secondary Skeletal muscle strength Change in the biceps brachii force production 10 weeks
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