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Virtual Reality in Lower Limb Adult Burn

Efficacy of Wii Fit Training on Lower Limb Burn in Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04677764
Acronym
adultburn
Enrollment
34
Registered
2020-12-21
Start date
2016-05-01
Completion date
2019-08-20
Last updated
2020-12-21

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

Conditions

Burns

Keywords

burns, lower limb burns, virtual reality

Brief summary

To investigate the potential effects of Wii fit rehabilitation programs on functional capacity, mobility, balance and muscle strength in lower limb burn patients after hospital discharge.

Detailed description

The use of virtual reality technology in burn conditions improved joint flexibility and reduced pain associated with physical therapy, dressing changes, and wound debridement. However, the primary concern of burn rehabilitation is not only survival but also maximizing functional outcome and decreasing the time for return to work.

Interventions

OTHERStandard of care

physical therapy and occupational therapy exercises either at their own home or a gym

OTHERvirtual reality

Wii Fit balance board (Nintendo Inc., Kyoto, Japan).

Sponsors

Cairo University
CollaboratorOTHER
Qassim University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

A blinded author to group allocation collected the outcome measures at baseline and after 12 weeks of intervention period.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* adult with a deep partial thickness or a full thickness burn in the lower extremities. * induced by either a scaled or a flame thermal burn. * total body surface area (TBSA) more than 40%. * age ranged from 18 to 40 years. * recent hospital discharge.

Exclusion criteria

* Infection. * Diabetes. * inhalation injury. * Fracture. * degenerative joint diseases of the lower extremities. * peripheral nerve diseases. * Pre-established psychologically and physically disorders.

Design outcomes

Primary

MeasureTime frameDescription
high mobility assessment toolat baselineused to assess mobility assessment after burn injuries. It is a valid and reliable unidimensional assessment tool which includes nine functional tasks, where 0 = inability to do and 4= able to do extremely well, with a total score of 54. Each Functional task is rated on a five-point performance scale with higher scores indicate a higher level of performance
Lower Limb Functional Indexat baselinea valid and reliable patient self-reported questionnaire to assess lower limb function for patients with a burn injury. It is consisted of fifteen general and ten lower-limb specific items that assess the functional status of the patients during the last 2-3 days. The scoring options for the LLFI Items are Yes=1 point, Somewhat= 0.5 point and No= 0 point. The scoring points are added and then multiplied by four for a total score of functional limitation. The total score of the LLFI ranges from 0 (maximum limitation) to 100 (no limitation or normal functional status)
Timed-up and go testat baselineused to evaluate functional mobility of the patients that requires both static and dynamic balance. The TUG test is a basic mobility assessment tool which records the time taken to stand up from a chair, walk 3 meters, return and sit down on the chair. The TUG test was performed with a standardized instruction, asking patients to walk as fast as possible during the test. All participants performed the TUG test from a standard chair (seat height of approximately 46 cm) with back support and no arms

Secondary

MeasureTime frameDescription
The six-minute walk testat baselineused to assess functional exercise capacity of the participants. The 6-MWT was performed in a 30-meters flat corridor according to the American Thoracic Society guidelines. Patients were asked to walk as far as possible in the 30-m corridor during the 6-min period. Standardized verbal encouragement is given to the patients during the 6-MWT. At the end of the test, the walking distance was measured. The predicted values of 6-MWT were calculated according to age and gender
Isokinetic Muscle Strength Assessmentat baselineassessed by A Biodex dynamometer (Biodex Medical System, Shirley, NY, USA). The values of knee flexors and extensors muscle peak torque of dominant leg were measured regardless the location of burns at an angular velocity of 150°/seconds, hip angle of 100° and patient were supported with a securing belt placed over the mid- thigh, pelvis and trunk. Three sub-maximal repetitions were allowed for the patient without any load as a warm-up. The patient then carried out 10 of maximum voluntary muscle contractions continuously without rest and the highest values were recorded for analysis.
Stability Indexat baselineassessed by A Biodex Balance System (Biodex Medical Systems, Shirley, NY) which consists of a movable balance platform that provides 20° surface tilt through 360° range of motion. The platform interfaces with computer software that enables the device to serve as an objective assessment of balance. All measurements were performed at level eight of stability, and the test duration was set at 20 seconds for three successive trials.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026