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Идёт набор NCT07384754

Foot Strengthening to Improve Balance and Gait in Older Adults

Без фазы С лечением Minimalist Footwear Traditional Foot Exercise Program Foot Strengthening Device (ToePro) Control Condition

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Minimalist footwear, Foot strengthening exercises, ToePro foot strengthening device.
Кому может быть актуально
Состояния в реестре: Minimalist Footwear, Traditional Foot Exercise Program, Foot Strengthening Device (ToePro), Control Condition. Базовые параметры: 45 лет — 85 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Evaluation of a Novel Foot Strengthening Device for Improving Fall Risk, Balance, and Gait With Age

Обзор

The goal of this clinical trial is to learn whether different foot-strengthening strategies can improve foot strength, balance, walking ability, and fall-related outcomes in middle-aged and older adults (ages 45-85 years). The main questions it aims to answer are: * Does foot strength change from baseline after an 8-week foot-strengthening intervention? * Do balance, gait, and physical function improve following different foot-strengthening approaches? Researchers will compare minimalist footwear use, a foot exercise program, a foot-strengthening device (ToePro), and no intervention to see if these interventions lead to greater improvements in foot strength, balance, gait, and fall-related outcomes than no intervention. Participants will: * Complete baseline and post-intervention laboratory testing of foot strength, balance, physical function, and walking gait * Perform foot strengthening exercises or wear minimalist footwear (if applicable) five days/week for eight weeks * Complete daily logs to record intervention compliance

Подробное описание

This randomized controlled trial evaluates the effects of multiple foot-strengthening interventions on foot strength, balance, gait, and fall-related outcomes in adults aged 45-85 years. Participants are recruited using a unified screening process and randomized to one of several intervention arms across two coordinated protocols. Interventions include habitual use of minimalist footwear, a prescribed foot exercise program, use of a commercially available foot-strengthening device (ToePro), or a no-intervention control condition.

All participants complete two in-laboratory data collection sessions conducted at baseline and after an 8-week intervention period. Laboratory assessments include measurements of foot morphology, intrinsic and extrinsic foot muscle strength, standing balance, physical function, and walking gait. Participants also complete standardized questionnaires assessing physical activity, balance confidence, fall history, and foot health. A follow-up questionnaire assessing physical activity, footwear use, foot health, and falls is administered six months after the intervention period.

During the 8-week intervention period, participants assigned to an active intervention are instructed to follow standardized intervention protocols specific to their assigned group. Physical activity levels during the intervention period are monitored for all groups using wearable activity tracking devices that record metrics such as daily step count and time spent in moderate-to-vigorous physical activity. These data are used to characterize habitual physical activity during the intervention period and to account for potential differences in overall activity levels between groups.

Intervention compliance is monitored throughout the 8-week period using self-reported compliance surveys. Participants report adherence to assigned footwear use, exercise sessions, or device use according to their intervention group. Compliance data are used to quantify adherence to the prescribed intervention protocols and to support interpretation of intervention effects.

Data from both protocols are pooled to allow direct comparison of the effects of different foot-strengthening strategies on foot strength, balance, gait, and fall-related outcomes in middle-aged and older adults.

Вмешательства

  • Устройство Minimalist footwear
    Habitual use of low-cushion, low-structure footwear designed to increase intrinsic foot muscle engagement during daily activities.
  • Поведенческое Foot strengthening exercises
    Home-based exercises including toe flexion, toe press, and arch-control movements performed several times per week.
  • Устройство ToePro foot strengthening device
    A dense foam exercise platform designed to strengthen intrinsic foot muscles through loaded toe press exercises in lengthened muscle positions.

Первичные конечные точки

  • Change From Baseline in Hallux Flexion Strength (Curl) [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Lesser Toes Flexion Strength (Curl) [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Hallux Flexion Strength (Press) [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Lesser Toe Flexion Strength (Press) [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Gait Kinetic Variables [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Joint Angles during Gait [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Joint Range of Motion During Gait [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Stance Time During Gait [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Step Length During Gait [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Cadence During Gait [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
Вторичные конечные точки (6)
  • Change From Baseline in IMU-Derived Gait Acceleration Magnitude [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Footwear Minimalism (Minimalist Index) [Срок оценки: Baseline]
  • Intervention Compliance Survey Responses [Срок оценки: Throughout the 8-week intervention period]
  • FitBit-Derived Moderate-to-Vigorous Physical Activity (MVPA) [Срок оценки: Throughout the 8-week intervention period]
  • Change From Baseline in International Physical Activity Questionnaire (IPAQ) Scores [Срок оценки: From enrollment to the end of the intervention at 8 weeks]
  • Change From Baseline in Sedentary Behavior Questionnaire (SBQ) Scores [Срок оценки: From enrollment to the end of the intervention at 8 weeks]

Критерии участия

Критерии включения

  • Healthy adults: age 45-85 years old
  • Able to walk without an assistive walking device or lower limb prosthesis
  • No history of foot or ankle surgery
  • No history of regular minimalist footwear use
  • No foot or ankle issues for which study activities may be contraindicated
  • BMI <= 40

Критерии исключения

  • Deemed unfit for physical activity by the Physical Activity Readiness Questionnaire (PAR-Q)
  • Current or history of an unresolved musculoskeletal, neurological, cardiovascular, pulmonary/respiratory, metabolic, renal condition, disease, or problem
  • Use of orthotics in daily (i.e., non-athletic) footwear
  • Pregnancy
  • Any other disease or problems that may affect movement or the ability to exercise even at a low intensity

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

США · 1 центр
  • School of Public Health-Bloomington — Bloomington

Идентификаторы

NCT: NCT07384754 · 26834, 23946

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗