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Clinical Trials/NCT01543984
NCT01543984
Completed
Phase 1

Efficacy of "Tailored Physical Activity" on the Number of Sick Days: a Randomized Controlled Trial in Health Care Workers That Have Experienced Pain Related to the Spine or Upper Body

University of Southern Denmark1 site in 1 country54 target enrollmentStarted: January 2012Last updated:
ConditionsPain

Overview

Phase
Phase 1
Status
Completed
Enrollment
54
Locations
1
Primary Endpoint
Self-reported number of sick-days

Overview

Brief Summary

The purpose of this study is to test the effect of "Tailored Physical Activity" on the number of sick-days.

The hypothesis is that "Tailored Physical Activity" is superior in efficacy on sick-days.

Detailed Description

Health care workers have high prevalence of musculoskeletal pain. Pain in the back and neck and other musculoskeletal disorders are the leading cause for long-term sick leave.

This study test the effect of "Tailored Physical Activity" on self-reported days on sick leave and parameters regarding pain, function and quality of life respectively on the body function and participation level of health care workers which have experienced musculoskeletal pain related to the back or upper body.

A minimum of 44 health care workers in DK-Sønderborg Municipality will be randomized for "Tailored Physical Activity" or a reference group.

Primary endpoint is 3 months and 12 months follow-up.

Study Design

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

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Health care workers in municipality of Sønderborg that have experienced musculoskeletal pain related to the spine or upper body.

Exclusion Criteria

  • Medically safety.

Outcomes

Primary Outcomes

Self-reported number of sick-days

Time Frame: 3 months

"How many days have you in total been on sick leave because of musculoskeletal troubles (such as ache, pain, discomfort)during the last three months" ((0 days, 1-7 days, 8-30 days, 30 days).

Secondary Outcomes

  • Hand-grip strength(12- months follow-up)
  • Body weight, waist circumference, hip circumference(12 months follow-up)
  • Questionnaire(12 months follow-up)
  • Aerobic capacity(12 months follow-up)
  • Self-reported number of sick-days(12 months follow-up)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lotte Nygaard Andersen

Ph.d. fellow

University of Southern Denmark

Study Sites (1)

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