Reducing Loneliness of Older Adults in Long Term Care Facilities Through Collaborative Augmented Realities

NCT ID: NCT06179225

Last Updated: 2025-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-22

Study Completion Date

2025-05-22

Brief Summary

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The goal of this clinical trial is to test the use of head-mounted display (HMD) augmented reality (AR) in older adults residing in long term care communities. The main questions it aims to answer are: what is the feasibility, acceptability, and satisfaction of HMD AR vs two-dimensional audio-video communication? Older adults and their designated family member will complete HMD AR activities in 8 session visits over 4 weeks. Researchers will compare HMD AR to 2-D audio-visual (AV) comparison group on feasibility, acceptability, and satisfaction with the interactive communication technology.

Detailed Description

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For both interventions, the bandwidth within the family members' homes will be measured and a hotspot created if necessary to facilitate data streaming. For each session, a trained research assistant (RA) will be physically present at the Long-term Care (LTC) to troubleshoot for technological issues. The RA will observe the staff member establish the Interactive Communication technology (ICT) connection between the older adult and family member, assisting as needed. The RA and staff member will remain within the room; the RA will monitor for technological issues. The staff member will monitor the older adults' reactions.

HMD-AR Intervention Experimental Setup. For the older adults, equipment set-up will be in a dedicated room at the LTC that allows for environmental overlays. Equipment includes two Kinect cameras, one HMD and one E4 wrist sensor that the older adult will wear to measure stress through physiological sensing. The family member will be consulted for placement of the 2 Kinect cameras in their home.

AR Activities. At least one meal session and one activity session will be conducted. The remaining sessions will consist of activities based on the preference of the older adult-family member. Staff will be trained to turn on the headset, computers, and ensure communication connection between the older adult and family member.

2D Audio-visual Intervention The 2D audio-visual sessions will take place in a dedicated room at the LTC. Staff will initiate the connection between the older adult and family member. In the unlikely event a family member does not have a device for the 2D audio-visual visits, a computer tablet will be supplied for use during the study.

Conditions

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Loneliness

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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HMD AR

Pairs of older adults with their designated family members who geographically apart will perform collaborative activities using HMD AR in 8 sessions over 4 weeks.

Group Type EXPERIMENTAL

HMD AR

Intervention Type BEHAVIORAL

Older adults will wear head mounted display to engage in collaborative augmented reality activities: sharing a meal, playing board games, and decorating home.

2-D Audio-Visual

Pairs of older adults with their designated family members who geographically apart will perform collaborative activities using 2-D Audio-Visual in 8 sessions over 4 weeks.

Group Type ACTIVE_COMPARATOR

2-D AV

Intervention Type BEHAVIORAL

Older adults will use 2-D AV to engage with family members at a distance.

Interventions

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HMD AR

Older adults will wear head mounted display to engage in collaborative augmented reality activities: sharing a meal, playing board games, and decorating home.

Intervention Type BEHAVIORAL

2-D AV

Older adults will use 2-D AV to engage with family members at a distance.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* age 60 and older
* residing at LTC greater than 3 months

Exclusion Criteria

* unable to provide assent or consent
* unable to understand or speak English
* physical impairment that impedes participation
* terminally ill
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute on Aging (NIA)

NIH

Sponsor Role collaborator

Vanderbilt University

OTHER

Sponsor Role lead

Responsible Party

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Nilanjan Sarkar

Professor, Mechanical Engineering

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nilanjan Sarkar

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt University

Locations

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Vanderbilt University

Nashville, Tennessee, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Informed Consent Form

View Document

Other Identifiers

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R21AG078480

Identifier Type: NIH

Identifier Source: secondary_id

View Link

078480

Identifier Type: -

Identifier Source: org_study_id

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