Healthy Subjects (HS)NCT07860619
Reactive Balance Training in Augmented Reality for Older Adults
A study testing Reactive balance training with augmented reality group and Treadmill walking in people with Healthy Subjects (HS), run by The Hong Kong Polytechnic University at 1 site in Hong Kong.
Trial summary
This is a single-blinded study. The participants will be equally randomized to either the reactive balance training with augmented reality (RBT+AR) group or the control (treadmill walking) group. Read more about this study
- Who is it for?
- Ages 60 years and older
- Conditions the study is for
- Healthy Subjects (HS)
- What is being tested?
- Reactive balance training with augmented reality group and Treadmill walking
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 36 participants
- Where
- 1 siteHong Kong
- Study dates
- 27 Jul 2026to 1 Sep 2027
- Phase
- Interventional
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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.
Who cannot join
- 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)
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- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Hong Kong1 site, 1 recruiting
- Recruiting
The Hong Kong Polytechnic University
Hong Kong
Sau Lan Tsang, PhD, +852 3400 8965, charlotte-sl.tsang@polyu.edu.hk
About this study
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
This is a single-blinded study. The participants will be equally randomized to either the reactive balance training with augmented reality (RBT+AR) group or the control (treadmill walking) group. Changes in postural stability, functional mobility/strength, balance performance, quality of life, balance confidence, muscle activation, and executive function following RBT+AR compared to treadmill walking only will be investigated.
Read the detailed description
This randomized controlled trial will recruit thirty-six community-dwelling older adults with increased fall risk. The participants will be equally randomized to either the RBT+AR group or the control group. The RBT+AR group will receive two sessions of treadmill-based RBT with 224 forward and backward perturbations, simulating tripping and slipping, while walking with AR headsets, and the control group will receive two sessions of treadmill walking without perturbation and AR. Between-group differences in behavior will be examined before and after training to identify training-induced changes in postural stability. Retention of the changes in the postural stability will be assessed four months after the training period. Incidents of falls will be followed up for 12 months after training.
- Conditions
- Healthy Subjects (HS)
- Being tested
- Reactive balance training with augmented reality group, Treadmill walking
- Keywords
- Reactive Balance Training, Augmented Reality
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Reactive balance training with augmented reality groupBehavioural
It will be two sessions of treadmill-based RBT with 240 forward and backward perturbations, simulating tripping and slipping, while walking with augmented reality headsets. Each session will last approximately one hour. Participants will be instructed to recover their balance and continue walking after each perturbation.
Treadmill walkingBehavioural
It will be a two sessions training with each session lasting for approximately an hour. The same training duration and format will be used as the experimental group, except that no perturbations and augmented reality will be induced during the treadmill walking.
| Study group | Role | What they receive |
|---|---|---|
| Reactive balance training with augmented reality group | Experimental | The group will receive two sessions of treadmill-based reactive balance training with 240 forward and backward perturbations, simulating tripping and slipping, while walking with augmented reality headsets. Receives: Behavioral: Reactive balance training with augmented reality group |
| Control group | Active comparator | The group will receive two sessions of treadmill walking without perturbation and augmented reality. Receives: Behavioral: Treadmill walking |
What is being measured
The primary outcome is the main question the study is designed to answer.
Postural stability
Postural stability at the recovery steps after the perturbation will be calculated as the distance between the absolute center of mass (CoM) position in an anteroposterior direction relative to the closest edge of the Base of Support (BoS) normalized by foot length. The absolute CoM position and BoS position will be traced by the motion capture system synchronized with the force plates embedded underneath the slip-treadmill belts.
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Secondary outcomes (13)
Generic balance ability
Generic balance ability will be assessed by the Brief-BESTest. Brief-BESTest can challenge balance across anticipatory postural adjustments, postural responses, sensory orientation and stability in gait, allowing for comprehensive examination of improvements that occur in reactive control. As a shortened version of the BESTest, the Brief-BESTest is an 8-item balance assessment containing 1 item for each of the 6 subsections of the BESTest.
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Mobility
Mobility will be assessed by Timed Up and Go test and Dual-Task Timed Up and Go test (in the unit of seconds)
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention
Number of real-life falls
The number of real-life falls in months after randomization will be recorded. Fall circumstances and related injuries will be required via phone contact. A fall is defined as an event resulting in a person unintentionally coming to rest on the ground or other lower level, not as the result of a major intrinsic event (e.g., syncope, stroke, or overwhelming hazard such as an earthquake).
Measured: 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, and 12 months after the intervention.
Dynamic balance
Dynamic balance will be assessed by Alternative Step Test (in the unit of seconds).
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Balance confidence
Balance confidence will be measured with the Chinese version of the shortened version of Activities-specific Balance Confidence Scale (ABC-6). The scale value is from 0 to 100, with higher values representing higher balance confidence.
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Functional lower body strength
Functional lower body strength will be assessed by Five-time Sit to Stand Test (in the unit of seconds).
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Cognitive flexibility and executive function
Cognitive flexibility and executive function will be assessed by Trial Making Tests A and B (in the unit of seconds).
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Cognitive impairment
Cognitive impairment will be assessed by Abbreviated Mental Test (AMT). AMT is a 10-item test, with a 10-point scale. A score less than 6 suggests a significant cognitive deficit.
Measured: Pre-intervention.
Depressive symptoms
Depressive symptoms will be assessed by Five-Item Geriatric Depression Scale. Participants will be asked to answer 5 questions as yes or no. The answer "no" for the first question and "yes" for the other four questions will be evaluated for depression.
Measured: Pre-intervention.
Personality traits
Personality traits assessed by Ten-Item Personality Inventory. It has 10 items, each item adopts a 5-level score of 1 (Disagree strongly) to 5 (Agree strongly), and a higher dimension score indicates a stronger individual's personality proneness.
Measured: Pre-intervention.
Generic preference-based quality-of-life
Generic preference-based quality-of-life will be assessed by five-level EuroQol five-dimensional questionnaire (EQ-5D-5L). The EQ-5D-5L essentially consists of 2 parts: the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS).
In the EQ-5D descriptive system, each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. Each health state is identified by a five-digit code, with 11111 representing the best and 55555 the worst possible health state.
In the EQ CAS, the scale value is from 0 to 100, with higher values representing higher balance confidence.
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Muscle activations
Muscle activations will be assessed by surface electromyography using an electromyography system (Trigno IM, Delsys Inc., Natick, MA, USA). Fourteen electrodes are placed bilaterally over erector spinae, rectus abdominis, gastrocnemius medialis, biceps femoris, rectus femoris, tibialis anterior, and gluteus medius according to the SENIAM guidelines (www.seniam.org) by the physical therapist.
Measured: Pre-intervention, 1 week after intervention and 4 months after intervention.
Physical activity
Physical activity will be assessed by the Physical Activity Scale for the Elderly. This questionnaire will ask participants to recall their activity over the last 7-days. Activity types include sitting, walking, sport/recreation, exercise, occupational and household. A total score for physical activity can be calculated using these answers and the predetermined weights associated with each activity.
Measured: Pre-intervention, and 4 months after intervention.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Oct 2026
- Study start27 Jul 2026
- Primary completion31 Jan 2027 (estimated)
- Study completion1 Sep 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Healthy Subjects (HS)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- The participants will be equally randomized to the RBT+AR group or the control (treadmill walking) group.
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 36 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The Hong Kong Polytechnic University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07860619
- Sponsor's protocol ID
- HSEARS20260423001
- Status last verified
- Jul 2026
- First submitted
- 1 Oct 2026
- Last updated
- 6 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No