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Sensorimotor Exercises in Virtual Reality Platform in Individuals With Human T-lymphotropic Virus

P

Pedreira, Érika, M.D.

Status

Completed

Conditions

HTLV-1

Treatments

Other: Video game

Study type

Interventional

Identifiers

NCT02877030
PedreiraE

Details and patient eligibility

About

Testing the effectiveness of an exercise protocol engines sensory performed through a virtual reality platform in individuals infected with HTLV-1

Full description

Crossover randomized clinical trial to be conducted with people having a previous diagnosis of HTLV-1, they can remain in standing position without assistance. They will be excluded from those presenting amputation of the lower limbs, pregnancy, psychiatric disorders, rheumatic or orthopedic diseases, other neurological disorders associated and those that are experiencing difficulty in understanding the assessment tools used. They will also be recruited to a comparative group, healthy individuals, matched for sex, age and education level. It will be performed three assessments, before randomization, after 10 weeks and after 20 weeks, which will be evaluated in balance, functional mobility, gait and posture. The participants infected with HTLV-1, will be divided into two groups by random distribution, a group will begin the treatment protocol with video game immediately after the first evaluation and the other after ten weeks, with the crossing of the groups . Concealment of allocation will be guaranteed to the examiners who will have no contact with the physiotherapist who will apply the exercise protocol and the team member responsible for drawing. Patients will also be instructed to maintain confidentiality of the entry in the exercise program to other patients and examiners.

Enrollment

42 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • people having a previous diagnosis of HTLV-1, which can remain in standing position without assistance.

Exclusion criteria

  • amputation of the lower limbs, pregnancy, psychiatric disorders, rheumatic or orthopedic diseases, other neurological disorders associated and those that are experiencing difficulty in understanding the assessment tools used.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

42 participants in 3 patient groups

Test control group
Experimental group
Description:
Start the sensorimotor exercises protocol with video game immediately after the first evaluation
Treatment:
Other: Video game
Control test group
Active Comparator group
Description:
Start of sensorimotor exercises with video game protocol after ten weeks
Treatment:
Other: Video game
comparison group
No Intervention group
Description:
No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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