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Live Long Walk Strong (LLWS) Rehabilitation Program: What Features Improve Mobility Skills

Not Applicable
Completed
Conditions
Mobility Limitation
Interventions
Other: Live Long Walk Strong rehabilitation program
Registration Number
NCT04026503
Lead Sponsor
VA Office of Research and Development
Brief Summary

This study is being performed to evaluate the efficacy of the Live Long Walk Strong rehabilitation program in Veterans 50 years and older. This study will also examine the features of the program that contribute to improved gait speed.

Detailed Description

Due to COVID-19, currently completed a virtual version of the LLWS intervention study.

The investigators are currently recruiting for the original study design in-person.

This study is a 4 year phase II randomized clinical trial study design. This study will provide important information about the mechanisms that contribute to meaningful improvement in mobility, the benefits of a novel mode of physical therapy care, and the duration of treatment effect.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
198
Inclusion Criteria
  • Veteran
  • Aged 50 and older
  • Community dwelling
  • Ability to speak and understand English
  • Usual gait speed 0.5 m/s- 1.0 m/s Activity modifications and access to telehealth rehabilitation
Exclusion Criteria
  • Presence of a terminal disease

  • A major medical problem, unstable chronic condition, or psychiatric disorder that interferes with safe and successful testing and training

  • Myocardial infarction or major surgery in previous 3 months

  • Planned major surgery

  • Baseline short physical performance battery score less than 4

  • Use of a walker

  • Modified mini mental status examination score less than or equal to 77

  • Presence of a significant disease specific impairment such as:

    • peripheral neurologic impairment
    • orthopedic impairment
    • visual impairment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
8 week wait list controlLive Long Walk Strong rehabilitation program8 week wait list then followed by 8 weeks of the Live Long Walk Strong rehabilitation program
Live Long Walk StrongLive Long Walk Strong rehabilitation program8 week rehabilitation program
Primary Outcome Measures
NameTimeMethod
Gait Speedwithin 2 weeks, 8 weeks, 16 weeks follow up

Gait speed change will be assessed within 2 weeks post intervention and then in 8 and 16 weeks of subsequent follow-up.

Virtual only pilot assessing the feasibility of the LLWS program in a virtual format.

Secondary Outcome Measures
NameTimeMethod
Lower Extremity Powerwithin 2 weeks, 8 weeks, 16 weeks follow up

Lower extremity power measure will be assessed at 3 time points post intervention. Power will be assessed via a keiser machine (force) and stair climb test (seconds).

Gait Variabilitywithin 2 weeks, 8 weeks, 16 weeks follow up

Gait variability will be measured at 3 time points post intervention. Gait variability will be assessed via zeno gait mat measurement of step length, step width and other measures of gait quality captured via the pkmas software within the zeno gait mat.

Trunk Muscle Endurancewithin 2 weeks, 8 weeks, 16 weeks follow up

Trunk muscle endurance will be measured at 3 time points post intervention. Trunk endurance will be assessed via saunders table through time (seconds) held in a fixed position.

Trial Locations

Locations (1)

VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA

🇺🇸

Boston, Massachusetts, United States

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