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Clinical Trials/NCT03294447
NCT03294447CompletedNot Applicable

The Association Between Fear of Falling and Fall Prevention Interventions Offered by an Occupational Therapist in a Geriatric Primary Care Setting

Rush University Medical Center1 site in 1 country13 target enrollmentStarted: November 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
13
Locations
1
Primary Endpoint
The Change of Falls Efficacy Scale-International (FES-I), standardized measure for fear of falling

Study Overview

Brief Summary

Purpose of the study: To identify if an intervention focused on decreasing fear of falling (FOF) in a geriatric primary care setting implemented by an occupational therapist (OT) has the potential to decrease falls and improve physical, psychological and social factors related to FOF.

The primary research question: Is there an association between fear of falling among geriatric populations and fall prevention interventions that are offered by occupational therapist in a geriatric primary care setting?

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •cognitively intact with a score of 29/30 or higher on the Orientation Log (standardized assessment tool)
  • •living in the community
  • •English speaking
  • •had a fall or near fall in the past year

Exclusion Criteria

  • •received OT services within the past 2 months

Arms & Interventions

Fall Prevention Intervention by OT

Experimental

Fall prevention interventions implemented by an OT in a geriatric primary care setting for a client immediately following the provider visit within the office.

Intervention: Fall Prevention by the Occupational Therapist (Behavioral)

Outcomes

Primary Outcomes

The Change of Falls Efficacy Scale-International (FES-I), standardized measure for fear of falling

Time Frame: One Time visit: 30-50 minutes

The outcome measure is the change between the pre FES-I and post FES-I

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lydia Royeen

Senior Occupational Therapist

Rush University Medical Center

Study Sites (1)

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