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Accidental FallNCT05829369

Intrinsic Foot Muscle Strengthening Interventions for Older Adults

A study testing Intrinsic foot muscle strengthening exercises and Minimal footwear with prescribed walking in people with Accidental Fall, run by Springfield College at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Falls are the leading cause of injury in adults over age 65. Muscle weakness in the foot can lead to foot and toe deformities such as collapsed arches or bunions, which have been found to contribute to falls in adults over age 65. Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
Conditions the study is for
Accidental Fall
What is being tested?
Intrinsic foot muscle strengthening exercises and Minimal footwear with prescribed walking
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
90 participants
Where
1 siteUnited States
Study dates
16 Dec 2022to 30 Sep 2025
Phase
Interventional
Are there results?
None posted in the registry

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 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • Can ambulate household distances (16 meters) with or without an assistive device
  • Have fall risk based on a "yes" to any of the Three Key Questions Do you feel unsteady when standing or walking? Do you worry about falling? Have you fallen in the past year? OR
  • Have a fall risk based on Timed Up and Go score (> 12 seconds)

Who cannot join

  • poor foot sensation (Semmes-Weinstein)
  • lower extremity amputations
  • lumbar spine or lower extremity injury or surgery in the past 6 months
  • impaired cognitive ability to follow verbal or written instructions (MMSE)
  • vestibular disorders
  • based on self-report and/or the Vestibular Screening Tool (score > 4)
  • participation in a fall prevention program in the previous 6 months

Trial locations and contacts

1 site in 1 country.

United States1 site, 1 recruiting
  • Springfield College

    Springfield, Massachusetts, 01027

    Erin Futrell, 413-748-3590, efutrell@springfieldcollege.edu

    Recruiting

Other trials in United States

About this study

Official title: The Effects of Intrinsic Foot Muscle Strengthening Interventions on Balance, Proprioception, Foot Structure, and Fall Risk in Adults Over Age 65

Falls are the leading cause of injury in adults over age 65. Muscle weakness in the foot can lead to foot and toe deformities such as collapsed arches or bunions, which have been found to contribute to falls in adults over age 65. The current research study aims to investigate the effectiveness of two simple and affordable foot strengthening methods that may make a major impact on balance and fall prevention in older adults.

Read the detailed description

Background: Falls are the leading cause of injury in adults 65 years and older. While causes of falls are multifactorial, foot function plays a vital role. The intrinsic foot muscles (IFM), those that originate and insert within the foot, provide stability and sensory input important for balance. Weakness or disuse of the IFM in older adults can contribute to faulty foot and toe alignment, which have been cited as independent predictors of falls. Wearing minimally cushioned footwear or performing strengthening exercises that target the IFM may improve these muscles' strength, endurance, proprioceptive qualities, and foot/toe structure, which may improve functional mobility and balance in older adults, and thus, prevent falls.

Purpose: The purpose of the proposed research is to analyze the effects of two IFM strengthening interventions (minimal footwear use or strengthening exercises) on IFM strength, proprioception, foot/toe structure, balance and functional mobility, and fall risk in older adults.

Design: Randomized control trial with an effectiveness-implementation hybrid design Type I

Methods: Adults ages > 65 years who can ambulate household distances with or without an assistive device who are determined to be at risk for falls will be invited to participate. Individuals with poor foot sensation, vestibular disorders, lower extremity amputation, injury or surgery to the lower extremities or lumbar spine in the previous 6 months, impaired cognitive ability to follow verbal and written instructions, and those who have participated in a fall prevention program in the past 6 months will be excluded. Following informed consent and initial screening, participants will be randomly allocated to one of three intervention groups (n=90, 30/group):

  1. intrinsic foot muscle strengthening exercises
  2. minimal footwear prescribed walking
  3. control (will receive a fall prevention brochure and seated active motion exercises)

Participants will be encouraged to perform interventions 5 days/week for 16 weeks. After an initial in-person instruction session, participants will have 1 follow-up meeting to review instructions, after which they will receive bimonthly phone calls as a reminder to adhere to the intervention and to record any falls and related details. Participants will be asked to record intervention performance, daily step count (measured by pedometer), and falls in provided diaries. Balance, functional mobility, and fall risk will be measured using the Mini-BesTest, proprioception will be measured using the Lower Extremity Position Test, foot and toe structure will be measured using navicular drop and valgus angle of the 1st metatarsophalangeal joint. Cross sectional area (cm2) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, and quadratus plantae muscles will be measured using ultrasound imaging. Measures regarding balance and functional mobility, proprioception, foot/toe structure, and muscle cross sectional area will occur at baseline, 8 and 16 weeks, and 1 year. Following the 16-week intervention period, participants will be encouraged to continue their intervention twice per week. Ongoing falls diaries and bimonthly phone calls from researchers will occur for 12 months after baseline to record long-term fall rate (falls per person per year). In addition, a process evaluation will be performed regarding participant impressions of the interventions and other study activities to inform future research and clinical implementation.

Data Analysis: a 4 group x 4 time point repeated measures analysis of covariance (ANCOVA) will be used to assess changes in balance, and functional mobility, proprioception, foot/toe structure, and muscle cross sectional area. Falls data will be measured as the rate of falls per person in a 12-month period beginning with the date of the baseline measure, and change in fall risk status will be assessed using Mini-BesTest scores. Implementation data will undergo both quantitative and qualitative analyses.

Significance: Intrinsic foot muscle strengthening interventions have seldom been studied in older adults and their effects and mechanism are not established. This will be the first study to assess the effects of these interventions on proprioception in older adults, the first to use ultrasound imaging measurement following intrinsic foot muscle strengthening in older adults, and the first study to analyze the long-term effects on falls after the performance of these specific interventions. The interventions assessed in this research proposal are simple, safe, and affordable and may have a major impact on functional mobility and reduction of falls for older adults.

Conditions
Accidental Fall
Being tested
Intrinsic foot muscle strengthening exercises, Minimal footwear with prescribed walking, Control
Keywords
older adults, falls, feet, balance, proprioception, muscle strength

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intrinsic foot muscle strengthening exercisesOther

    participants will perform specific toe and foot motions that recruit plantar intrinsic foot muscles, 3 sets of 10 for each exercise, 5 days per week

  • Minimal footwear with prescribed walkingOther

    Participants will be provided minimal footwear. They will walk 30 minutes per day, 5 days per week, and be prescribed a gradual increased time in minimal footwear during daily activities (up to a maximum of 7.5 hours per day).

  • ControlOther

    Participants will perform seated upper and lower extremity active range of motion activities 5 days per week. They will also be given a brochure on fall prevention tips.

Study groups in NCT05829369
Study groupRoleWhat they receive
Intrinsic foot muscle exerciseExperimentalThis group will perform intrinsic foot muscle strengthening exercises
Receives: Other: Intrinsic foot muscle strengthening exercises
Minimal FootwearActive comparatorThis group will perform prescribed walking in and daily wear of minimally cushioned footwear
Receives: Other: Minimal footwear with prescribed walking
ControlSham comparatorThis group will be given a falls prevention brochure and seated upper extremity and lower extremity active range of motion activities.
Receives: Other: Control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Mini BesTest scores

    a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)

    Measured: Baseline

  2. Change in Mini BesTest scores

    a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)

    Measured: 8 weeks post intervention

  3. Change in Mini BesTest scores

    a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)

    Measured: 16 weeks post intervention

  4. Change in Mini BesTest scores

    a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)

    Measured: 1 year post intervention

  5. Change in intrinsic foot muscle cross-sectional area/strength

    real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot

    Measured: Baseline

  6. Change in intrinsic foot muscle cross-sectional area/strength

    real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot

    Measured: 8 weeks post intervention

  7. Change in intrinsic foot muscle cross-sectional area/strength

    real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot

    Measured: 16 weeks post intervention

  8. Change in intrinsic foot muscle cross-sectional area/strength

    real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot

    Measured: 1 year post intervention

Secondary outcomes (12)
  1. Change in hallux valgus angle

    a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot

    Measured: Baseline

  2. Change in hallux valgus angle

    a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot

    Measured: 8 weeks post intervention

  3. Change in hallux valgus angle

    a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot

    Measured: 16 weeks post intervention

  4. Change in hallux valgus angle

    a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot

    Measured: 1 year post intervention

  5. Change in navicular drop measure

    the Navicular Drop Test will measure the amount of foot pronation in sitting and standing

    Measured: Baseline

  6. Change in navicular drop measure

    the Navicular Drop Test will measure the amount of foot pronation in sitting and standing

    Measured: 8 weeks post intervention

  7. Change in navicular drop measure

    the Navicular Drop Test will measure the amount of foot pronation in sitting and standing

    Measured: 16 weeks post intervention

  8. Change in navicular drop measure

    the Navicular Drop Test will measure the amount of foot pronation in sitting and standing

    Measured: 1 year post intervention

  9. Change in proprioception measure

    The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting

    Measured: Baseline

  10. Change in proprioception measure

    The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting

    Measured: 8 weeks post intervetion

  11. Change in proprioception measure

    The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting

    Measured: 16 weeks post intervention

  12. Change in proprioception measure

    The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting

    Measured: 1 year post intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Apr 2023
  2. Study start16 Dec 2022
  3. Primary completion30 Sep 2025 (estimated)
  4. Study completion30 Sep 2025 (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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized control trial with an effectiveness-implementation hybrid design Type I
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05829369
Sponsor's protocol ID
U01CE003495
Status last verified
Apr 2023
First submitted
31 Jan 2023
Last updated
25 Apr 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Intrinsic foot muscle strengthening exercises and Minimal footwear with prescribed walking in people with Accidental Fall, run by Springfield College at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 25 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Erin Futrell, PhD (413-748-3590, efutrell@springfieldcollege.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Mini BesTest scores (time frame: Baseline). The study lists 8 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Apr 2023.

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