Child, Only, Hemophilia, Musculoskeletal Diseases or Conditions
Conditions
Keywords
Physical Therapy, Exercise, Muscle strength
Brief summary
"Being able to participate in games and activities with their friends" is one of the things that matters most to boys with haemophilia. At present, there is a lack of robust evidence to determine whether muscle strengthening exercise can improve or negatively affect outcomes for young children with haemophilia. With the help of boys with haemophilia, their parents and physiotherapists the investigators have developed an exercise programme designed to increase muscle strength. Using this intervention the investigators will undertake a single-blinded, two-arm pragmatic randomised controlled trial (RCT) of a 12-week intervention verses usual care of boys with haemophilia aged 6-12 years of age.
Detailed description
Children are born with haemophilia. Females carry the disorder and usually males are affected. It is a disorder affecting 1:10000 people where the blood does not clot normally, leading to bleeding into muscles and joints. As a result, muscles become weak. Joints become painful and difficult to move. "Being able to participate in games and activities with their friends" is one of the things that matters most to boys with haemophilia. "What is the role of exercise for both prevention and treatment of joint damage in haemophilia?" is one of the top unanswered questions that concern patients, carers and healthcare professionals most. At present, there is a lack of robust evidence to determine whether muscle strengthening exercise can improve or negatively affect outcomes for young children with haemophilia. With the help of boys with haemophilia, their parents and physiotherapists the investigators have developed an exercise programme designed to increase muscle strength. The investigators think the exercise programme might have an effect on pain and movement in participants joints, help them participate in games and activities with their friends and improve their health in the long term. The investigators recently showed the exercise programme had no harmful effects, was acceptable to children with haemophilia and that the participants were willing to participate in a study to answer the question, "does muscle strengthening help improve the long term health of children with haemophilia?" To answer this question, the investigators will allocate 66 boys with haemophilia to a group that is asked to complete the 12-week exercise routine to strengthen their leg muscles and another 66 boys to a group that does not do the exercises. The boys will be allocated at random, so that each boy has an equal chance of being in either group. Random allocation helps ensure that two similar groups of boys will be compared. The investigators will monitor the boys throughout the study by measuring their muscle strength, how far they can walk in six-minutes and time taken to ascend and descend 12 steps. The investigators will also record how physically active the boys are using a wrist band as well as how satisfied they are with their health. The study will be managed by a group of health care professionals and researchers with experience and expertise in carrying out this type of research. In addition, the investigators will include parents of boys with haemophilia in the research team to provide invaluable lived experience of living with the condition. So that people hear about what the investigators learn in the study, the investigators will report the findings to other researchers using journals, relevant health care professionals through face to face meetings, and children with haemophilia and their families through newsletters and presentations at Haemophilia Society meetings.
Interventions
OTHERExercise
12-week exercise intervention
OTHERUsual Care
usual care
Sponsors
East Kent Hospitals University NHS Foundation Trust
Great Ormond Street Hospital for Children NHS Foundation Trust
University of Kent
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)
Masking description
It is impossible to blind those in receipt and those delivering the intervention as to group allocation. However, it will be possible, although perhaps challenging, to blind the assessor to group allocation. Consequently, we will attempt a single blind approach in which the participant and physiotherapists delivering the intervention will be encouraged to withhold their group allocation from the assessors collecting data.
Intervention model description
A single-blinded, two-arm pragmatic randomised controlled trial
Eligibility
Sex/Gender
MALE
Age
6 Years to 12 Years
Healthy volunteers
No
Inclusion criteria
• Children aged 6-12 years, with severe or moderate haemophilia A or B
Exclusion criteria
* von Willebrand disease * past history of fracture or trauma to the lower limb * orthopaedic surgery * acquired brain injury or any other disturbance of the central nervous system; joint or muscle bleed in the lower limb in the past 6 weeks * presence of lower limb pain or unable to fully comply with verbal instructions.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Muscle strength of the dominant knee extensors at 24 weeks | 24-weeks | Maximum isometric torque (Newton.metres/kilogram of body weight) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Muscle strength of the ankle plantarflexors and non-dominant knee extensors at 24 weeks | 24 weeks | maximum isometric torque (Newton.metres/kilogram of body weight) |
| Bleeding episodes and coagulation factor usage | 24 weeks | Number of bleeding episodes (number) and amount of coagulation factor used for treatment (number) |
| Six-minute timed walk (6MTW) | 24 weeks | Distance walked in 6 minutes (metres) |
| Timed up and down stairs (TUDS) | 24 weeks | Time taken to ascend and descend a flight of 12 steps (seconds) |
| Participation in physical activity | 24 weeks | Time spent in moderate-vigorous physical activity physical activity (MVPA) |
| Child Health Utility 9D (CHU9D) | 24 weeks | a paediatric preference based measure of health related quality of life (utility values on the 0.0 to 1.0 quality adjusted life year scale) Higher score represent higher adjusted life years. |
Countries
United Kingdom
Contacts
STUDY_CHAIRDavid Stephensen, PhD
East Kent Hospitals University NHS Foundation Trust
Outcome results
None listed