NCT07213388

Brief Summary

The purpose of this research project is to examine the feasibility and acceptability of a virtual reality-based physical activity (VRPA) intervention for inactive adults compared to more traditional forms of physical activity. The project will explore the relationship between VRPA engagement and cognition, biological measures (calories burned, heart rate, and active minutes), rate of perceived exertion, flow, affect, and enjoyment in physical activity as well.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
61

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

February 19, 2025

Completed
8 months until next milestone

First Posted

Study publicly available on registry

October 8, 2025

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 22, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 22, 2025

Completed
Last Updated

January 16, 2026

Status Verified

January 1, 2026

Enrollment Period

1.1 years

First QC Date

February 19, 2025

Last Update Submit

January 15, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Pace of participant recruitment

    enrollment rate of 6 participants per month

    Up to 24 months

  • Number of participants willing to continue using the assigned exercie modality

    Willingness to continue using the exercise modality to which the participants were assigned and self-report enjoyment from engaging in the assigned exercise.

    Day 1

  • Percentage of participants who complete the required tasks in each condition

    Are participants able to complete the required tasks

    Day 1

Secondary Outcomes (9)

  • Changes in Heart Rate

    Day 1

  • Self-reported measures of "flow" associated with the assigned conditions

    Day 1

  • Changes in affect

    Day 1

  • Rate of percieved exertion

    Day 1

  • Changes in Stroop Color and Word Test

    Day 1

  • +4 more secondary outcomes

Study Arms (3)

Control

ACTIVE COMPARATOR

Participants will sit quietly while listening to the same music playlist that is played during the VRPA condition.

Behavioral: Control

Treadmill

EXPERIMENTAL

Participants will walk on a treadmill while listening to the same playlist that is played during the VRPA condition.

Behavioral: Treadmill

Virtual Reality Physical Activity (VRPA)

EXPERIMENTAL

Participants will wear the VR headset and complete one pre-selected exercise session.

Behavioral: VRPA

Interventions

VRPABEHAVIORAL

Effects of virtual reality physical activity on outcomes

Virtual Reality Physical Activity (VRPA)
TreadmillBEHAVIORAL

Effects of treadmill walking with music on outcomes

Treadmill
ControlBEHAVIORAL

Effects of music while sitting on outcomes

Control

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be inactive (i.e., do not meet physical activity guidelines)
  • have no current neurological, psychiatric, sensory, or motor impairment, and normal or corrected-to-normal vision (only thin wire glasses or contacts can be used)
  • have no history of motion sickness
  • have the ability to exercise based on the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) (Warburton et al., 2019)
  • Have not fallen to the point of injury in the last 6 months.
  • Be willing to wear an activity tracker
  • years,

You may not qualify if:

  • Struggle to use operate a VR headset
  • Cannot read
  • Have concerns about balance/falling while using a VR headset,
  • Unable to provide informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rowan University

Glassboro, New Jersey, 08028, United States

Location

MeSH Terms

Interventions

Exercise Test

Intervention Hierarchy (Ancestors)

Heart Function TestsDiagnostic Techniques, CardiovascularDiagnostic Techniques and ProceduresDiagnosisRespiratory Function TestsDiagnostic Techniques, Respiratory SystemErgometryInvestigative Techniques

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Participants are not told their group assignment until after completing the pre-session assessments.
Purpose
TREATMENT
Intervention Model
FACTORIAL
Model Details: Three group, randomized trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 19, 2025

First Posted

October 8, 2025

Study Start

September 1, 2024

Primary Completion

October 22, 2025

Study Completion

October 22, 2025

Last Updated

January 16, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will share

Researchers can request deidentified data sets after the research team has published all planned analyses related to this research.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
September 2026 until August 2036
Access Criteria
Researchers will be able to access the data upon request. The PI will securely share the requested IPD.

Locations