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Clinical Trials in the USA / NCT07092176
Recruiting Not applicable

Steady Stride Fall Prevention Protocol vs Standard of Care

NCT07092176 · tracked via the Priya Life Science USA tracker
Sponsor
Steady Strides: Fall Prevention and Stroke Rehabilitation Medical Institute
Phase
Not applicable
Started
2026-04-01
Last updated
2026-04-29

Condition(s) studied

Fall PreventionFalls

Investigational drug(s) / intervention(s)

Steady Strides

Steady Strides: Participants in the control arm will receive a one-time assessment by a trained research assistant at baseline and once more at 2 month follow up. Research assistant will measure and document the specified demographic and clinical variables to be compared between the control and intervention groups. Participants in the intervention arm will receive a multifactorial intervention, including: Medical Intervention: Provided by physician(s) and/or nurse practitioners (NPs) or physician assistants (PAs) trained in the Steady Strides fall prevention protocol via the hybrid online and in person course on the Steady Strides fall prevention protocol . Rehabilitation Intervention: Provided by occupational therapists (OTs) and physical therapists (PTs) trained through a hybrid online and in person course on the Steady Strides fall prevention protocol

Study summary

Falls are the leading cause of preventable morbidity and mortality in community dwelling older US adults (65 years old and older) . This is a research study to evaluate the comparative effectiveness of the structured physiatry-based Steady Strides Fall Prevention Protocol compared to the standard of care treatment provided by primary care providers in preventing falls in community-dwelling older adults.

Eligibility

Sex
ALL
Min age
65 Years
Max age
Healthy volunteers
No
Inclusion Criteria: Age: Participants must be community-dwelling older adults aged 65 years or older. Fall History: Participants must have reported experiencing at least two falls in the six months prior to the intake visit. Independence: Participants must report the ability to drive independently at the time of the intake visit and ambulate at least 10 feet with or without an assistive device (e.g. cane or walker, wheelchair ambulators are not included). Participants must report their ability to independently make medical decisions and sign their medical paperwork, including consent to participate in the study. Setting: Participants must reside in a community setting, not in a long-term care facility or hospital. Language: Participants must report ability to speak, read and comprehend English fluently. Exclusion Criteria: No additional exclusion criteria beyond those specified in the inclusion criteria. All individuals who meet the inclusion criteria are eligible to participate in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Steady Strides Baltimore Maryland Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07092176 on ClinicalTrials.gov ↗ ← All trials in the USA