Reactive Balance Training with Augmented Reality for Older Adults
Official title: The Combined Effects of Reactive Balance Training in an Augmented Reality Environment on Postural Stability in Community-dwelling Older Adults With an Increased Risk of Falling: A Randomized Controlled Trial
Run by The Hong Kong Polytechnic University · NCT07860619 · Data updated 2026-11-12
This study tests whether reactive balance training using augmented reality helps older adults who are at risk of falling, compared with regular treadmill walking.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 60 Years and up |
| Sex | All |
| Enrollment | 36 (estimated) |
| Sponsor | The Hong Kong Polytechnic University Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | July 27, 2026 |
| Main results expected | January 31, 2027 |
| Study ends | September 1, 2027 |
| Registry record updated | October 6, 2026 |
| Trial ID | NCT07860619 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Community-dwelling adults aged 60+ who have fallen or feel unsteady and can walk 30 minutes on level ground, with adequate cognitive ability and Cantonese or Mandarin communication.
✕Probably not a fit
Individuals unable to safely participate in treadmill-based training or with contraindications to the assessment procedures may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this randomized, single-blinded trial, 36 community-dwelling adults aged 60 and older at increased fall risk will be assigned to either reactive balance training with augmented reality (RBT+AR) or treadmill walking without AR. The RBT+AR group will complete two treadmill sessions that simulate tripping and slipping with AR headsets, while the control group does two treadmill walking sessions without perturbations or AR. Researchers will compare changes in postural stability, mobility, strength, balance performance, quality of life, balance confidence, muscle activation, and executive function before and after training, and again four months later for retention. Falls will be tracked for 12 months after training to assess long-term impact. The study is conducted under single-blind conditions and will analyze between-group differences to identify training-induced effects.
Why it matters
Potential benefit: If successful, older adults may experience improved balance and reduced fall risk through AR-enhanced training.
How similar studies have gone: Previous perturbation-based balance training approaches have shown potential benefits, though AR-enhanced methods are relatively novel in this population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Community-dwelling adults aged 60 years old or older * Able to communicate effectively in Cantonese or Mandarin * Able to walk independently on level ground for at least 30 minutes * Abbreviated Mental Test (Hong Kong version) scores \> 6 * Have fallen in the preceding year, have concerns about falling, or feel unsteady while walking or standing. Exclusion Criteria: * Uncorrected vision or hearing impairment * Osteoporosis * Have a history of hip or knee replacement * Resting blood pressure ≥ 160/100 mmHg * Resting heart rate exceeds the 60-100 beat/min normal range * Have musculoskeletal conditions causing pain or functional limitation that would preclude safe performance of study procedures (e.g., acute fracture) * Have cardiovascular conditions that may pose risks during training or assessment (e.g., uncontrolled arrhythmias) * Have mental health conditions impairing decision-making capacity or ability to comply with study instructions (e.g., psychosis) * Have neurological conditions affecting balance, coordination in a way that would increase safety risk (e.g., Parkinson's disease) * Participating or planning to participate in another fall prevention program.
Where it's running
-
The Hong Kong Polytechnic University
Hong Kong, Hong Kong Recruiting
Study contacts
- Study coordinator: Sau Lan Tsang, PhD
- Email: charlotte-sl.tsang@polyu.edu.hk
- Phone: +852 3400 8965
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Bioequivalence comparison between YHP2508B and YHR2602 in healthy adults
This study tests whether YHP2508B and YHR2602 deliver similar amounts of the drug in healthy adults after a single dose.
-
Bioequivalence test of two drugs in healthy adults
This study tests whether YHP2508A and YHR2601 are bioequivalent in healthy volunteers.
-
How the body responds to exercise with low oxygen in healthy adults
Researchers test how healthy men and women respond to different exercise types while breathing air with varying oxygen levels.
-
IS M8969 safety and PK/PD in healthy and at-risk adults
This early-phase study tests ISM8969 versus placebo to see if it is safe, well tolerated, and how the body handles and responds to it in healthy adults and obese adults at risk for heart disease.
-
Ear-based vagus nerve stimulation to improve reaction time
Researchers will try a short, noninvasive electrical stimulation of the vagus nerve at the ear to see if it shortens reaction time in healthy adults.
-
Single ascending-dose safety and response test of SYH2070 injection in healthy adults
This test gives a single subcutaneous dose of SYH2070 to healthy adults with mildly high triglycerides to see whether it is safe, how the body handles it, and whether it causes early biological effects compared with placebo.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.