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Effect of Physiotherapy in Patients Presenting to the Emergency Department After a Fall (EPAC-I)

University Hospital Basel logo

University Hospital Basel

Status

Completed

Conditions

Fear of Falling

Treatments

Other: physiotherapeutic intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05156944
2021-02165 am21Bingisser2;

Details and patient eligibility

About

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.

Enrollment

104 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

104 participants in 2 patient groups

intervention group
Experimental group
Description:
The 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.
Treatment:
Other: physiotherapeutic intervention
control group
No Intervention group
Description:
The control group will receive written information on the expected course of the condition, written instructions on self-management and written instructions on exercises for daily self-guided therapy.

Trial contacts and locations

1

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Central trial contact

Roland Bingisser, Prof. Dr. med.; Henk B. Riedel

Data sourced from clinicaltrials.gov

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