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Recruiting NCT06657989

Optimal Intensity of Reactive Balance Training for Healthy Older Adults

No phase Interventional Accidental Falls

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Reactive balance training, Walking.
Who it may be relevant to
Registry conditions: Accidental Falls. Basic parameters: 65 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Falls in daily life are a serious risk for older adults. A new type of balance training, called reactive balance training (RBT) involves people losing balance many times so that they can practice fast balance reactions, like stepping reactions. Differences in training program features might explain differences in the results of previous RBT studies. Training intensity is the difficulty or challenge of the training program. It would be valuable to know if high-intensity RBT improves balance reactions quickly. The main goal of this study is to see if more intense RBT improves balance reactions faster than less intense RBT. The investigators will compare how quickly people improve balance reactions between high- and moderate-intensity RBT, and between RBT and a control program that does not include RBT. The investigators will also test if the improvements in balance reactions last after the training program is over. The secondary goals are to understand exactly how balance reactions improve with training, and to determine if people who complete RBT improve their general balance skills, and falls efficacy more than people who do not complete RBT.

Interventions

  • Behavioral Reactive balance training
    Reactive balance training involves clients experiencing repeated balance perturbations so that they can practice and improve control of reactions to avoid falling after a loss of balance.
  • Behavioral Walking
    Overground walking

Primary outcome measures

  • Number of reactive steps [Time frame: Two weeks]
Secondary outcome measures (7)
  • Step initiation time [Time frame: One week and 12 weeks post-training]
  • Step execution time [Time frame: One week and 12 weeks post-training]
  • Step length [Time frame: One week and 12 weeks post-training]
  • Braking impulse [Time frame: One week and 12 weeks post-training]
  • Mechanical margin of stability [Time frame: One week and 12 weeks post-training]
  • Balance evaluation systems test [Time frame: One week and 12 weeks post-training]
  • Falls efficacy scale - International [Time frame: One week, 12 weeks, and 12 months post-training]

Eligibility criteria

Inclusion criteria

  • Community-dwelling older adults (65-80 years old)

Exclusion criteria

  • Unable to stand independently without upper-limb support for >30 seconds and/or walk independently (without a gait aid) for ≥10 metres;
  • Diagnosed neurological condition that could affect balance control (e.g., stroke, Parkinson's disease);
  • Score below normative values on the Montreal Cognitive Assessment;
  • Score below age-matched normative values for sensory and motor function, as assessed using the FallScreen battery;
  • Have insufficient English language comprehension such that they cannot understand instructions;
  • Have contraindications to reactive balance training such as severe osteoporosis; and/or
  • Are currently attending physiotherapy or supervised exercise.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

Canada · 1 center
  • University Health Network — Toronto

Identifiers

NCT: NCT06657989 · 24-5665

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗