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Clinical Trials/NCT03501147
NCT03501147CompletedNot Applicable

The Effect of a Brief Daily Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.

University of Valencia2 sites in 1 country37 target enrollmentStarted: April 17, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
37
Locations
2
Primary Endpoint
Pain overall status: Standard 7-point patient global impression

Study Overview

Brief Summary

The prevalence and consequences of musculoskeletal pain is considerable among healthcare workers, allegedly due to high physical work demands of healthcare work.

Performing physical exercise at the workplace together with colleagues may be more motivating for some employees and thus increase adherence. On the other hand, physical exercise performed during working hours at the workplace may be costly for the employers in terms of time spend. Thus, it seems relevant to perform a brief intervention. This study is intended to investigate the difference between the effect of workplace-based physical exercise (using elastic bands and body weight exercises) and a group control on musculoskeletal pain, physical exertion during work, physical function, need for recovery, self-rated use of analgesics, and work ability among healthcare workers.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • Healthcare Workers at the Hospital
  • Informed consent

Exclusion Criteria

  • Unable to perform exercises

Arms & Interventions

Intervention

Experimental

15 minutes of resistance training at the work place every day

Intervention: Resistance training (Other)

Control

No Intervention

Usual work

Outcomes

Primary Outcomes

Pain overall status: Standard 7-point patient global impression

Time Frame: 2 days after the end of intervention (POST)

Standard 7-point patient global impression of pain collected at the endpoint

Secondary Outcomes

  • "Need for recovery scale" after work(2 days after the end of intervention (POST))
  • Physical function(2 days after the end of intervention (POST))
  • Perceived physical exertion(2 days after the end of intervention (POST))
  • Workability Index(2 days after the end of intervention (POST))
  • Self-rated use of analgesics(2 days after the end of intervention (POST))
  • Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)(2 days after the end of intervention (POST))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

José Casaña Granell

Doctor

University of Valencia

Study Sites (2)

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