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Evaluation of application, safety and motor and cognitive effects of video game Nitendo Wii Fit Plus® in frail elderly

Evaluation of applicability, safety and outcomes motor and cognitive of video game Nitendo Wii Fit Plus® in frail elderly

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-823rst
Enrollment
Unknown
Registered
2016-07-11
Start date
2015-09-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Elderly with frailty syndrome

Interventions

The study will consist of two phases: First stage will be a pilot study to analyze the feasibility and safety of the game Nintendo Wii Fit Plus in frail elderly. The pilot study will consist of five
however, we believe that will participate in this step 20 frail elderly (10 in each group). Subjects will be randomized by drawing lots into two groups: experimental group and control group. Participa
Other

Sponsors

Faculdade de Medicina da Universidade de São Paulo
Lead Sponsor
Faculdade de Medicina da Universidade de São Paulo
Collaborator

Eligibility

Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: Frail elderly and pre frail will be selected with 60 or older, diagnosed with frailty syndrome according to the criteria of Fried. The elderly should not present neurological or orthopedic diseases that promote the inability to remain in bipedalism and wade; with normal or corrected visual acuity measured by Snellen chart; Good hearing is clinically assessed by the whisper of the test; who did not have previous experience with the Nintendo Wii Fit® and who accept sign the Informed Consent and Informed of the study.

Exclusion criteria

Exclusion criteria: The elderly will be excluded that during the study period, submit any clinical change that makes it impossible to perform physical exercises in standing position, as cardiorespiratory, orthopedic or neurological disorders; elderly unable to interact with the game; and in the second phase of the study will exclude elderly who are missing for more than three consecutive sessions without replacement.

Design outcomes

Primary

MeasureTime frame
In the first phase of the study will be the primary outcomes applicability and safety of the training with Nintendo Wii Fit after six intervention sessions. The applicability will be quantified upon accession of the elderly to training. The safety will be evaluated through records of the possible adverse effects such as vertigo, dizziness, malaise, imbalances and others. To asses these negative effects we will realize the evaluation pre and post intervention the following parameters: blood pressure, oxygen saturation, heart rate and we will apply the BORG scale to analyses the subjective perception of the effort. After analyses of the first results and if the technique will applicable we will start the second phase of the study. In the second phase we will be evaluated the postural control with the Mini BesTest scale and the cognition with the MoCA scale.

Secondary

MeasureTime frame
The second outcomes will be: postural control evaluates by posturography (stability limit area (E), elliptical area and speed of oscillation) evaluated from the platform Neurocom Balance Manager®; quality of life by SF-36 scale; gaming performance through score records; gait by the scales Dynamic Gait Index and Functional Gait Assessment; functional capacity by Olders Americans Research and Services Multidimensional Functional Assessment Questionare (BOMFAQ); falls by International Falls Efficacy Scale; depression by GDS-15; records with falls during the study period; criteria fragility by Fried et. al.

Countries

Brazil

Contacts

Public ContactJosé Pompeu

Faculdade de Medicina da Universidade de São Paulo

j.e.pompeu@gmail.com+55 (11) 30917459

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 8, 2026