Effects of an Augmented Reality Exercise Program in Older Adults

NCT06549140 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-08-12

No results posted yet for this study

Summary

This research aims to examine the effects of an augmented reality (AR) exercise program on physical fitness (cardiorespiratory capacity, strength, balance, agility, and flexibility) and cognitive function (reaction time, decision-making, and memory).

Conditions

  • Augmented Reality Exercise Program
  • Traditional Exercise Program
  • Control Group

Interventions

OTHER

Augmented reality exercise program

Participants enrolled in an organized exercise program based on two weekly sessions of 45 to 60 minutes each for 12 weeks: one traditional session (group session) and one augmented reality (AR) session (individual session), both supervised by sports and exercise professionals. The AR session was designed to provide an entire exercise session targeting physical fitness components (cardiorespiratory capacity, strength, balance, agility, and flexibility) and cognitive function (reaction time, decision-making, and memory).

OTHER

Traditional exercise program

Participants enrolled in a traditional organized exercise program (group sessions) based on two weekly sessions of 45 to 60 minutes each for 12 weeks. These sessions are supervised by sports and exercise professionals, targeting physical fitness components (cardiorespiratory capacity, strength, balance, agility, and flexibility) and cognitive function (reaction time and decision-making).

Sponsors & Collaborators

  • Élvio Rúbio Gouveia

    collaborator UNKNOWN
  • Hildegardo Noronha

    collaborator UNKNOWN
  • Francisco Santos

    collaborator UNKNOWN
  • Mara Dionísio

    collaborator UNKNOWN
  • Eva Freitas

    collaborator UNKNOWN
  • Pedro Campos

    collaborator UNKNOWN
  • Paulo Bala

    collaborator UNKNOWN
  • Universidade da Madeira

    lead OTHER

Principal Investigators

  • Élvio Gouveia, PhD · University of Madeira

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
60 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-01-31
Primary Completion
2025-02-28
Completion
2025-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06549140 on ClinicalTrials.gov