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Effect of Physiotherapy in Patients Presenting to the Emergency Department After a Fall

Not Applicable
Completed
Conditions
Fear of Falling
Interventions
Other: physiotherapeutic intervention
Registration Number
NCT05156944
Lead Sponsor
University Hospital, Basel, Switzerland
Brief Summary

The aim of this monocentric, block-randomized, controlled, open-label, parallel-group study is to assess whether patients presenting to the emergency department (ED) with a fall within the past 7 days would benefit from a physiotherapy intervention, as compared to patients without physiotherapy intervention at the time of ED presentation. Primary objective of this study is to assess "fear of falling" 7 days after ED presentation with versus without a physiotherapy intervention.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
104
Inclusion Criteria
  • Written informed consent
  • Age ≥65
  • History of falls within the last 7 days
  • Presentation to the ED of the University Hospital Basel
Exclusion Criteria
  • Inpatient disposition after ED work-up
  • Immobilizing fractures of the lower extremities
  • Inability or contraindications to undergo the investigated intervention or follow the study procedures, e.g. due to certain neurological disorders (such as parkinsonism, hemiplegia, severe multiple sclerosis), language problems, psychological disorders, cognitive impairment
  • Prior enrolment in this trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
intervention groupphysiotherapeutic interventionThe study intervention is a brief physiotherapeutic assessment, a brief information on the expected course of the condition, and a brief instruction on self-management, including two exercises for daily self-guided therapy.
Primary Outcome Measures
NameTimeMethod
Change in short International Falls efficacy scale (sFES-I)At Day 0 and Day 7 ± 7 days

Change in the fear of falling between groups at day 7, measured by the short International Falls efficacy scale (sFES-I). It is a 7-item questionnaire where individuals are instructed to score their concern of falling during an activity on a 4 point Likert scale with 1 as not concerned at all and 4 as very concerned. The item scores are summed up to obtain a total, with a higher score indicating a higher fear of falling.

Secondary Outcome Measures
NameTimeMethod
Occurence of fallsDay 7 ± 7 days, Day 21 ± 3 days, Day 42 ± 3 days

Occurence of falls following randomization from patient recollection

Feasibility of the interventionAt Day 0

Feasibility of the intervention assessed by a questionnaire filled out by the physiotherapist

Change in short International Falls efficacy scale (sFES-I)At Day 0, Day 7 ± 7 days, Day 21 ± 3 days, Day 42 ± 3 days

Change in the fear of falling, measured by the short International Falls efficacy scale (sFES-I). It is a 16-item questionnaire where individuals are instructed to score their concern of falling during an activity on a 4 point Likert scale with 1 as not concerned at all and 4 as very concerned. The item scores are summed up to obtain a total, with higher the score, higher being the concern for falling.

Utilization of medical resourcesDay 7 ± 7 days, Day 21 ± 3 days, Day 42 ± 3 days

Comparison of the use of medical resources between both groups (ED visits, GP visits, hospitalization, physiotherapy, imaging; all since inclusion)

Satisfaction with ED work-upDay 7 ± 7 days

Patients' satisfaction with ED work-up assessed by questionnaire

Objective functional levels in the intervention groupAt Day 0 and Day 7 ± 7 days

Functional levels measured by SPPB in the intervention group

Trial Locations

Locations (1)

Department of Emergency Medicine, University Hospital Basel

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Basel, Switzerland

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