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Effects of an Augmented Reality Exercise Program in Older Adults

Effects of an Augmented Reality Exercise Program in Older Adults Physical Fitness and Cognitive Abilities

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06549140
Enrollment
30
Registered
2024-08-12
Start date
2025-01-31
Completion date
2025-04-30
Last updated
2024-08-12

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

Conditions

Augmented Reality Exercise Program, Traditional Exercise Program, Control Group

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).

Interventions

OTHERAugmented 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).

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

Élvio Rúbio Gouveia
CollaboratorUNKNOWN
Hildegardo Noronha
CollaboratorUNKNOWN
Francisco Santos
CollaboratorUNKNOWN
Mara Dionísio
CollaboratorUNKNOWN
Eva Freitas
CollaboratorUNKNOWN
Pedro Campos
CollaboratorUNKNOWN
Paulo Bala
CollaboratorUNKNOWN
Universidade da Madeira
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 95 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
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

MeasureTime frameDescription
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.

Contacts

Primary ContactCíntia França, PhD
cintia.franca@staff.uma.pt(+351)291209400
Backup ContactFrancisco Santos, Mac
francisco191santos@gmail.com(+351)291209400

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026