MedPath

Effects of an Augmented Reality Exercise Program in Older Adults

Not Applicable
Not yet recruiting
Conditions
Traditional Exercise Program
Control Group
Augmented Reality Exercise Program
Interventions
Other: Augmented reality exercise program
Other: Traditional exercise program
Registration Number
NCT06549140
Lead Sponsor
Universidade da Madeira
Brief 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).

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Participants of both genders
  • 60 years or older
  • Autonomous community-dwelling older adults
Exclusion Criteria
  • Neurological disorders
  • Cognitive impairment
  • Health limitations related to exercise participation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Augmented reality exercise programAugmented reality exercise programParticipants 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 a full exercise session targeting physical fitness components (cardiorespiratory capacity, strength, balance, agility, and flexibility) and cognitive function (reaction time, decision-making, and memory).
Traditional exercise programTraditional exercise programParticipants 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).
Primary Outcome Measures
NameTimeMethod
Physical fitnessTesting sessions will occur at baseline, at week 6, at week 13 and at week 18.

Physical fitness will be assessed using the fitness test battery proposed by Rikli \& Jones (1999), including: 30-s chair stand test to assess lower-body strength, arm curl test to evaluate upper-body strength, back scratch test to examine upper-body flexibility, chair seat and reach test to assess lower-body flexibility, 8-foot up-and-go test to assess agility and dynamic balance, and the 6-min walk test to evaluate aerobic endurance.

Physical activityParticipants enrolled in exercise programs will be monitored using accelerometry. Individual data will be collected in all exercise sessions (total of 48 sessions).

Physical activity levels will be measured using accelerometry during each exercise session.

Body compositionTesting sessions will occur at baseline, at week 6, at week 13 and at week 18.

Body composition will be evaluated using the InBody 770, which allows a hand-to-foot biolectrical analysis. Bodyweight, body fat percentage, and fat-free mass will be used for analysis.

Cognitive functionThe assessment will be conducted at baseline, at week 6, at week 13 and at week 18.

Participants' cognitive function will be examined through the Cognitive Telephone Screening Instrument and the Mini Mental State Examination.

Secondary Outcome Measures
NameTimeMethod
SF-36 questionnaireThe assessment will be conducted at baseline and at week 13 after the intervention end.

The SF-36 questionnaire is used to assess the participant's health status of participants. It consists of 36 items that assess physical functioning, physical performance, physical pain, emotional functioning, vitality, mental health, social functioning, and general health. The higher the score, the better the participant's health.

© Copyright 2025. All Rights Reserved by MedPath