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Xbox Kinect Promote Physical Fitness and Lean Mass in Severely Burned Children (XboxBurn)

Q

Qassim University

Status

Completed

Conditions

Burns

Treatments

Other: Xbox training
Other: Control group

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The outcome measures included quadriceps muscle strength as measured using an isokinetic dynamometer, LBM is measured by DEXA and cardiopulmonary fitness was assessed by measuring VO2 peak during a standardized treadmill exercise test using the modified Bruce protocol. All outcome measures were evaluated immediately after discharge as baseline and after 12 weeks of intervention.

Full description

Forty healed pediatric burn patients (24 boys and 16 girls), aged 10 - 15 years, were enrolled from the outpatient clinic in the faculty of physical therapy, Cairo university, Egypt. The inclusion criteria were: total body surface area (TBSA) of 40-60%, being ambulatory without an assistant. The exclusion criteria included metabolic disorders, neuropathy, visual or vestibular disorders, amputation, participation in another study, any adverse medication reactions, history of epilepsy, loss of balance, and lower or upper limb deformity. All patients received similar standard medical care and treatment from the time of admission until the time of discharge.

Total burn surface area was assessed by the "modified Lund and Browder charts" method during excisional surgery immediately following hospital admittance. Informed written consent was obtained from each patient's guardian prior to enrollment.

All procedures were approved by the ethical committee of the faculty of physical therapy, Cairo university, Giza, Egypt. After consent was obtained, patients were randomly assigned to standard of care group (SOC) or Xbox training group (Xbox).

The Xbox group participated in a 12-week of routine physiotherapy program supplemented with Xbox training program (N=20). In contrast, the SOC group participated in the routine physiotherapy program (N=20).

A normal activity of daily living (ADL), diet and patient's lifestyle were maintained for all participants as much as possible.

Enrollment

40 patients

Sex

All

Ages

10 to 15 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • total body surface area (TBSA) of 40-60%.
  • being ambulatory without an assistant.

Exclusion criteria

  • metabolic disorders.neuropathy.
  • visual or vestibular disorders.
  • amputation.
  • participation in another study.
  • history of epilepsy.
  • loss of balance.
  • lower or upper limb deformity.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

40 participants in 2 patient groups, including a placebo group

Xbox training group
Experimental group
Description:
The study group received Xbox training plus routine physical therapy protocol treatment. The dose of Xbox training was 50 min, three times a week for 12 weeks, using the Xbox gaming system (Xbox 360 Kinect console; Microsoft Inc., Redmond, Washington, USA).
Treatment:
Other: Control group
Other: Xbox training
Control group
Placebo Comparator group
Description:
patients participated in a routine physical therapy protocol (RPTP) including joint range of motion exercises (ROM), muscle stretching technique, splinting, daily walking, and ADL training.
Treatment:
Other: Control group

Trial documents
1

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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