Learning From Falling: Perturbation-based Training to Prevent Falls in Older Adults
NCT ID: NCT04770103
Last Updated: 2023-05-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
16 participants
INTERVENTIONAL
2021-01-11
2022-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
An emerging fall prevention training regimen is perturbation-based training (PBT). PBT involves rapidly disrupting balance requiring the participant to take rapid steps to recover balance. This is commonly achieved on a laboratory treadmill equipped with a safety harness to prevent actual falls during training. By simulating "real-world" balance challenges such as slips and trips, PBT provides a direct means for learning how to recover balance and avoid falls. It has been demonstrated that with only a few PBT sessions, older adults make rapid and dramatic improvements in balance recovery performance, retain the skills long-term and potentially suffer fewer falls over extended periods. This study builds on the previous published work of the PI that describes the key factors related to differences in balance recovery performance, the neuro-motor coordination strategies used during successful and unsuccessful recovery, and currently unpublished pilot studies indicating the efficacy of PBT. To date studies have not directly compared BT regimes recommended by the American College of Sports Medicine (ACSM) against PBT, nor have they evaluated the influence of training on the incidence of real-world falls. In part this may be because PBT currently requires the use of expensive, laboratory treadmills and as such is not accessible by the average independent, community dwelling older adults. A specific randomized study is required and our overall purpose for this study is to compare the balance recovery performance of older adults following either BT or PBT, evaluate differences in the incidence of real-world falls, and develop a safe, effective and portable device for use in future community PBT training studies. The short-term goals are to determine the effect of PBT versus BT and the neuro-motor mechanism of improved recovery behavior.
Aim 1: To evaluate differences in balance recovery behavior in older adults following either balance training (BT) and perturbation-based training (PBT) and the incidence on real-world falls.
H1: Balance recovery performance will improve in both BT and PBT groups but will be significantly better in those completing PBT when compared to BT.
H2: Improvements in balance recovery behavior will be related to improved coordination and neuro-motor control strategies.
H3: Real world loss of balance events will be similar in both BT and PBT but incidence of resulting falls will be lower in the PBT group.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Fall Prevention in Older Adults Study
NCT03176511
Perturbation-Based Treadmill Training to Prevent Unrecovered Falls in Geriatric Patients
NCT06652828
Instrumented vs. Conventional Perturbation-based Balance Training for Fall Prevention
NCT04087512
Prevention of Falls in Older Adults by Specific and Progressive Balance Training
NCT03464825
"Stay Balanced" - Prevention of Falls in Older Adults - From Clinical Research to Clinical Practice
NCT02909374
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
1\) The main study The main study to investigate the difference between BT and PBT is a parallel-group randomized controlled trial with 6 months follow-up from baseline to determine the effect of PBT program on stepping behavior and fall incidence in community-dwelling older people. The study has been designed in accordance with the Consolidated Standards of Reporting Trials (CONSORT) statement48.
Participants, recruitment and screening Participants will consist of community-dwelling adults aged over 65 years without a recent history of falls (one or more falls in the past 12 months). All participants will be required to obtain medical clearance from their general practitioner prior to participation in the study. Exclusion criteria will be neurological, cardiovascular or musculoskeletal impairment that adversely affect balance or limit involvement in the intervention, diagnosis of dementia, cognitive impairment (score\<24 on Mini Mental State Examination after adjustment for age and years of education49), functional disability/limitation in activities of daily living (Score\>3 on Bayer Activities of Daily Living Scale50), osteoporosis, use of medication that affects balance or causes dizziness (e.g. psychotropics) and participation in supervised exercise one or more times per week.
Random allocation and concealment Randomization will be performed following baseline assessment by personnel not involved in recruitment, training or assessments. Participants will be informed that they will receive one of two treatments. Due to the nature of the intervention, research personnel administering the treatments cannot be blinded to group allocation. However, the personnel that perform the prospective falls evaluation will be blinded to group allocation.
Intervention BT group. This group will undertake 12 weeks of twice weekly BT in accordance with ACSM guidelines. Training will be conducted in small groups under the supervision of a trainer. Training will involve mobility, resistance and balance training components.
PBT group. The PBT protocol uses multi-directional surface translations to provoke rapid compensatory stepping responses to recover balance. The protocol is a modified version of the stepping (but not grasping) component of the PBT program described by Mansfield et al., which was designed to improve rapid stepping reactions and minimize foot collisions in accordance with well-established principles of motor learning including individualization, specificity, progressive overload, and variability of training. At each session the PBT group will experience multi- directional disturbances to standing posture (forwards, backwards, left, right) delivered via translations of a motorized treadmill. 24 perturbations will be administered in a random sequence (with variation in timing, magnitude and direction) and interspersed with 30 s treadmill walking. Successful recoveries during training will be followed by an increase in the degree of difficulty, whereas consecutive failures will result in a return to the perturbation intensity that had previously been performed successfully. Our pilot testing indicates that the prescribed peak accelerations on our motorized treadmill to within ±3% can be achieved. The occurrence of actual falls will be prevented via the use of a custom safety harness attached to an overhead cable instrumented with a force transducer used previously. One familiarization trial in each perturbation direction will be performed at 50% intensity at the beginning of the first training session. Training sessions will be terminated when the participant completes the planned number of trials or if the participant elects not to continue (e.g. feels tired, uncomfortable or unwell).
Primary outcome measures The tether-release54 test will be used to determine whether training effects generalize to balance recovery reactions that are not part of the intervention. Loss of balance will be induced by releasing participants from static forward lean postures corresponding to 15%, 20% and 25% of their body weight on a horizontal restraining tether in accordance with the PI's previous work groups published procedures. Participants will be instructed to attempt to regain balance by taking a single, rapid step. Full body kinematics and ground reaction forces will be recorded during all balance recovery tasks using a 3D motion capture system (12-camera Motion Analysis) and force platforms embedded in the ground (AMTI, Watertown, USA). Outcome measures will be margin of stability at touchdown of the stepping leg, step leg kinematics (step length and velocity) and trunk kinematics (trunk angle and trunk angular velocity). All analysis will be performed using OpenSim57 in accordance with the PI's and his previous research units published methods.
Secondary outcomes measures Falls frequency will be monitored over the 3 months of the intervention and following 3 months of follow up with monthly falls diaries. Participants will return monthly falls diaries (daily entries) to determine frequency, time, location and cause of falls and related injuries as per consensus recommendations for falls trials52.
OVERALL SUMMARY
The proposed investigation forms the basis of improved understanding of balance recovery training methods and are important steps for ongoing research into the efficacy of balance recovery training modes relative to reducing the incidence of falls. In particular, the proposed study is the necessary precursor to a large prospective study to evaluate the effect of balance recovery training on health and wellbeing of rural Montanans.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
BASIC_SCIENCE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Dynamic
Participants within the dynamic arm will receive either traditional balance training within ACSM guidelines or Dynamic Step training known as Perturbation based training (PBT). Outcome measures assessed will be Margin of Stability during dynamic step recovery when subjected to a forward loss of balance, along with static postural sway ( a measure of postural control not requiring a step recovery). Participants motivation, mental wellness, attitudes to exercise and fear of falling will be assessed prior to the intervention and 6 months following the intervention.
Balance recovery
Balance recovery by stepping ascertains the capability of the participant to recover when subjected to a loss of balance in the forward direction.
Attitudes towards exercise, fear of falling and mental wellness a psychosocial measures to ascertain the relationship between perceptions and physical capability.
Static
Participants within the static arm will receive only traditional balance training within ACSM guidelines. The outcome measure within the static arm is limited to static postural sway. Participants motivation, mental wellness, attitudes to exercise and fear of falling will be assessed prior to the intervention and 6 months following the intervention.
Postural Sway
Postural sway is a pseudo-static measure of postural control that evaluates a participants balance recovery ability when the perturbation does not require a dynamic step recovery.
Attitudes towards exercise, fear of falling and mental wellness a psychosocial measures to ascertain the relationship between perceptions and physical capability.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Balance recovery
Balance recovery by stepping ascertains the capability of the participant to recover when subjected to a loss of balance in the forward direction.
Attitudes towards exercise, fear of falling and mental wellness a psychosocial measures to ascertain the relationship between perceptions and physical capability.
Postural Sway
Postural sway is a pseudo-static measure of postural control that evaluates a participants balance recovery ability when the perturbation does not require a dynamic step recovery.
Attitudes towards exercise, fear of falling and mental wellness a psychosocial measures to ascertain the relationship between perceptions and physical capability.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Are aged 60 to 80 years
* Are living in the community
* Are a Non-smoker
* Do not have a recent muscle or joint injury
* Do not have a progressive musculoskeletal condition (arthritis, osteoporosis etc)
Exclusion Criteria
* If you regularly consume any analgesic or anti-inflammatory drug(s), prescription or non-prescription. If you are unsure about the drugs that you are taking, please ask us.
* You take medication that may make you dizzy or feel unbalanced, please consult with us regarding any prescribed medication you may be taking. Depending on the medication we may need screen you out of the study or ask that you to obtain clearance from your physician prior to being accepted into the study.
* A history of bone, joint, nerve, muscle problems or a current injury and are unable to obtain physician approval. This includes joint replacements or reconstructive surgery in the ankle, hip or knee joints.
* If you have had a stroke or have a heart condition for which moderate to vigorous exercise is contraindicated.
* If your doctor has told you that you should not do exercise.
60 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Montana State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Montana State University, Department of Health and Human Development
Bozeman, Montana, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DG020320
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.