Trial Radar AI | ||
|---|---|---|
Clinical Trial NCT07459439 (VR-C-REHAB) for Older Adults (65 Years and Older), Outpatient Treatment, Rehabilitation Frail Elderly Subjects is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
One study matched filter criteria
Card View
Feasibility of Virtual Reality-assisted Ergometer Cycling in Addition to Regular Rehabilitation During Municipality-based Inpatient Rehabilitation Care (VR-C-REHAB) 20 Exercise-Based Virtual
Clinical Trial NCT07459439 (VR-C-REHAB) is an interventional study for Older Adults (65 Years and Older), Outpatient Treatment, Rehabilitation Frail Elderly Subjects and is currently not yet recruiting. Enrollment is planned to begin on 9 March 2026 and continue until the study accrues 20 participants. Led by Horsholm Municipality, this study is expected to complete by 1 July 2026. The latest data from ClinicalTrials.gov was last updated on 9 March 2026.
Brief Summary
VR-C-REHAB is a single-group pilot and feasibility study examining the practicality of implementing virtual-reality-assisted ergometer cycling as an adjunct to usual municipal inpatient rehabilitation for older adults (≥65 years). Many individuals admitted to temporary inpatient care present with low physical activity levels and fluctuating motivation, reducing the achievable exercise dose. Virtual reality may enhanc...Show More
Detailed Description
Background and Rationale:
Elderly individuals with diminished physical capacity who are admitted to temporary inpatient rehabilitation often exhibit low levels of physical activity and motivation, which can adversely affect the exercise dose during their stay. Cycling is recognized as a safe and effective form of exercise; however, its implementation is often hindered by low commitment and fluctuating daily energy l...
Show MoreOfficial Title
Feasibility of Virtual Reality-assisted Ergometer Cycling in Addition to Regular Rehabilitation During Municipality-based Inpatient Rehabilitation Care: A Single-group Pilot- and Feasibility-trial - VR-C-Rehab
Conditions
Older Adults (65 Years and Older)Outpatient TreatmentRehabilitation Frail Elderly SubjectsPublications
Scientific articles and research papers published about this clinical trial:Other Study IDs
- VR-C-REHAB
NCT ID Number
Start Date (Actual)
2026-03-09
Last Update Posted
2026-03-09
Completion Date (Estimated)
2026-07-01
Enrollment (Estimated)
20
Study Type
Interventional
PHASE
N/A
Status
Not yet recruiting
Keywords
municipality-based inpatient rehabilitation care
Primary Purpose
Health Services Research
Design Allocation
N/A
Interventional Model
Single Group
Masking
None (Open Label)
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
ExperimentalIntervention | VR cycling * Intervention: 20 minutes of cycling with VR goggles in addition to regular treatment.
* Frequency: Three times weekly.
* Duration: Up to 4 weeks (dependent on discharge timing).
* Delivery: Supervised by physiotherapists or therapeutic staff according to local practices. |
Primary Outcome Measures
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Exercise Adherence: In percent | Definition: NumbercompletedVR-bicyclessessions/ NumberofferedVR-bicyclesessioner pr. participant, summarised and/or averaged for the entire cohort.
The feasibility goal is set at ≥75%. "Offered sessions" are defined as the planned three weekly sessions during the period the participant is admitted and available, excluding days with clearly documented contraindications or acute illness according to predetermined criteria. The reasons for lack of training will be explicitly described in the manual as "illness," covering biological illness or other admitted causes, and "demotivation," which encompasses reasons such as tiredness, demotivation, or discomfort. The actual cause will be described. | 4 weeks (at every exercise session) |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
1. Recruitment Rate: Percent | Definition: number whoconsent/ number asked, | Baseline testing (day 0) |
walk speed | 10MWT: M/s
o The time it takes the patient to walk 10 meters with a standing start, using walking aid if needed Measurements are taken at baseline (before the first session) and at completion (at discharge or week 4), converted to m/s. | baseline testing and follow up testing after ending the intervention( up to 4 weeks later) |
Motivation | Motivation: 0-10, 10 indicate highest degree of motivation
o Assessed by measuring the participant's motivation on a 0-10 scale at the start of each exercise session, recorded at the start of every session. | during every session from enrollment until end of intervention (max 4 weeks) |
Total Time Spent Cycling in minutes | Total Time Spent Cycling: Minutes
o Defined as the total bicycle time (minutes) completed with VR during the study period, calculated as the sum of minutes per session. | Week 4 (or after conclusion of the intervention if that happens before) |
Participation Assistant
Eligibility Criteria
Eligible Ages
Older Adult
Minimum Age
65 Years
Eligible Sexes
All
- Age ≥65 years
- Referred to rehabilitation during a stay at temporary inpatient care
- Assessed by a therapist as capable of participating in seated cycling (possibly supervised)
- Able to provide informed consent (with relevant support according to local guidelines, if necessary).
- Medical contraindications to moderate physical activity/cycling (e.g., unstable angina, uncontrolled arrhythmia, acute infection with significant impact)
- Severe dizziness/vestibular symptoms likely to be exacerbated by VR use
- Known photosensitive epilepsy or other conditions posing significant risk with VR stimulation
- Unresolved vision/perception issues or severe nausea rendering VR use unsuitable
- Participation in another intervention study that interferes with this intervention.
Study Responsible Party
Niklas Grundt Hansen, Principal Investigator, Research and developement therapist, Msc. PT, PhD Candidate, Horsholm Municipality
Study Central Contact
Contact: Niklas Grundt Hansen, PhD Candidate, +45 61277932, [email protected]
2 Study Locations in 1 Countries
Bispebjerg Hospital, Copenhagen, Denmark
Sundheds- og rehabiliteringscenter Hørsholm, Hørsholm, 2970, Denmark
Jane Larsen Department leader, Bsc., Dip BA, Contact, 20914541, [email protected]