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The Effects of Video Games in Stroke

U

Universidad de Burgos

Status

Completed

Conditions

Stroke
Hemiplegia

Treatments

Device: rehabilitation video game
Device: Commercial video game.

Study type

Interventional

Funder types

Other

Identifiers

NCT03896542
CEIC 1559

Details and patient eligibility

About

Aims: To establish whether the effectiveness of conventional treatment is increased when it is complemented with video-based therapy, whether specific rehabilitation or commercial after subacute stroke.

Design: Randomized clinical trial with pre / post-test and follow-up evaluation, assessor blinded study.

Methodology: Three different groups: conventional treatment, conventional treatment and commercial videogame, or conventional treatment and specific rehabilitation videogame. The three groups completed 12 sessions.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with stroke
  • Hemiplegia on the non-dominant side
  • More than 1 month since the stroke
  • Score 3 in the shoulder and 2 in the elbow in the modified Medical Research Council scale
  • No auditory alterations
  • No visual disturbances
  • Mini Mental Scale greater than or equal to 24

Exclusion criteria

  • Patients with unstable blood pressure or angina.
  • History of seizures.
  • Do not use video games

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

45 participants in 3 patient groups

Commercial video game
Experimental group
Description:
the group commercial video game received 30 minutes of conventional therapy plus 30 minutes of rehab training using Xbox Kinect-based games.
Treatment:
Device: Commercial video game.
Rehabilitation video game
Experimental group
Description:
the group rehabilitation video game received 30 minutes of conventional therapy plus 30 minutes of rehab games.
Treatment:
Device: rehabilitation video game
The control group
No Intervention group
Description:
The control group received 30 minutes of conventional therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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