Effects of Physical Training on Bone and Muscle Quality, Muscle Strength, and Motor Coordination in Children With NF1

NCT ID: NCT01058330

Last Updated: 2021-03-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-02-28
• Study Completion Date: 2014-02-28

Brief Summary

A physical training program will improve quality of life, participation in physical activity, motor coordination, muscle strength, and bone and muscle strength in children with neurofibromatosis type 1.

Detailed Description

Disorders of the Ras pathway have significant phenotypic overlap and include Noonan syndrome, Cardiofaciocutaneous syndrome (CFC syndrome), Legius syndrome, Costello syndrome and neurofibromatosis type 1 (NF1). NF1 is one of the most common genetic disorders presenting in childhood with an incidence of 1/3000. NF1 is associated with skeletal abnormalities such as short stature, scoliosis, and long bone fracture with non-union. We recently reported that children with NF1 have abnormalities of bone and muscle architecture as evidenced by decreased bone mineral density, decreased bone strength, and low muscle mass, all of which may predispose them to fractures and scoliosis (Stevenson et al., 2005, 2007, 2009). Our preliminary data show that children with NF1 have poor motor coordination and muscle strength, potentially secondary to abnormal neuromotor learning. We hypothesize that poor motor coordination and decreased muscle strength contribute to the osteopenia in NF1. Our objective is to identify effective and non-invasive strategies to improve motor coordination, muscle strength, and bone and muscle architecture in children with disorders of the Ras pathway, in hopes of decreasing fractures and improving physical activity levels. Plyometric physical training consists of quick, high-intensity, weight-bearing movements, and is an encouraging intervention for use in these children.

Conditions

Neurofibromatosis Type 1

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Plyometric physical training

Individualized plyometric training program to increase strength, coordination, and bone density.

Group Type: ACTIVE_COMPARATOR

Plyometric training program

Intervention Type: OTHER

The intervention is a year long individualized plyometric exercise training program. Examples of plyometric activities include jumping, hopping, running, and throwing. The number of plyometric exercises will increase gradually to prevent over training to a total of five lower extremity exercises and five upper extremity exercises

Control Group

This group will have no intervention

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Plyometric training program

The intervention is a year long individualized plyometric exercise training program. Examples of plyometric activities include jumping, hopping, running, and throwing. The number of plyometric exercises will increase gradually to prevent over training to a total of five lower extremity exercises and five upper extremity exercises

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Fulfill NIH clinical diagnostic criteria

Exclusion Criteria

• Visual impairment
• Participation in a simultaneous medical intervention trial
• Orthopedic procedure within the last 6 months.
• Pregnancy
• Home location greater than 3-4 hours drive time from Shriners Hospital
• Tibial pseudarthrosis

• Minimum Eligible Age: 4 Years
• Maximum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Thrasher Research Fund

OTHER

Sponsor Role: collaborator

University of Utah

OTHER

Sponsor Role: collaborator

Shriners Hospitals for Children

OTHER

Sponsor Role: lead

Responsible Party

David Stevenson, MD

Assistant Professor, Division of Medical Genetics, University of Utah

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

David Stevenson, MD

Role: PRINCIPAL_INVESTIGATOR

Shriners Hospitals for Children

Locations

Shriners Hospitals for Children, Salt Lake City

Salt Lake City, Utah, United States

University of Utah

Salt Lake City, Utah, United States

Countries

United States

Other Identifiers

SLC00038711

Identifier Type: -

Identifier Source: org_study_id