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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.

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Sites and contacts
Official record

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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
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
  • The Hong Kong Polytechnic University

    Hong Kong

    Sau Lan Tsang, PhD, +852 3400 8965, charlotte-sl.tsang@polyu.edu.hk

    Recruiting

Other trials in Hong Kong

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.

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 groups in NCT07860619
Study groupRoleWhat they receive
Reactive balance training with augmented reality groupExperimentalThe 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 groupActive comparatorThe 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.

  1. 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)
  1. 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.

  2. 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

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  1. First posted6 Oct 2026
  2. Study start27 Jul 2026
  3. Primary completion31 Jan 2027 (estimated)
  4. Study completion1 Sep 2027 (estimated)

Resources

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)
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

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