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Clinical Trials/NCT03831737
NCT03831737CompletedNot Applicable

Team-based Ergonomics Educational Model for Workplace WELLNESS Improvement: A Pilot Study

Milton S. Hershey Medical Center1 site in 1 country36 target enrollmentStarted: February 11, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
36
Locations
1
Primary Endpoint
SF-36

Study Overview

Brief Summary

This research is being done to explore the potential benefit of a physical therapist-guided stretching program on musculoskeletal pain and well-being.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •HMC/COM staff (faculty, residents, fellows, APPs, physical/occupational therapists, nurses, schedulers, etc.)
  • •At least 18 years old
  • •Willing and able to participate in all study procedures
  • •Willing and able to provide informed consent
  • •Group 2 subjects must have access to a computer with internet or an iPhone or Android smartphone

Exclusion Criteria

  • •Subjects who do not meet all inclusion criteria will be excluded from the study.

Arms & Interventions

Group 1: In-Person

Experimental

During the initial 3 month control period, subjects are asked not to begin any new exercise or stretching program during this time.

During the 3 month intervention period that follows, subjects will participate in in-person physical therapist-led instructional sessions three times per week. Each stretch will be performed twice, one on the left and one on the right. The therapist will describe what to do and briefly demonstrate each stretch. Stretches will be held for 45-60 seconds with therapist instructions and modification as needed based on subject technique.

Intervention: stretching exercises (Behavioral)

Group 2: Video

Experimental

During the initial 3 month control period, subjects are asked not to begin any new exercise or stretching program during this time.

During the 3 month intervention period that follows, subjects will complete sessions three times per week, led by a physical therapist and viewed remotely via pre-recorded video using a smartphone application.

Intervention: stretching exercises (Behavioral)

Outcomes

Primary Outcomes

SF-36

Time Frame: change from 3 month time point to 6 month time point

The 36-Item Short Form Health Survey (SF-36) is a set of generic, coherent, and easily administered quality-of-life measures.

CMDQ

Time Frame: change from 3 month time point to 6 month time point

The Cornell Musculoskeletal Discomfort Questionnaires (CMDQ) is a questionnaire based on previous published research studies of musculoskeletal discomfort among office workers.

Secondary Outcomes

  • SF-36(baseline, 3 months)
  • Modified Sit and Reach(baseline, 3 months, 6 months, change from 3 month time point to 6 month time point)
  • CMDQ(baseline, 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aiesha Ahmed

Assistant Professor, Neuromuscular Neurology

Milton S. Hershey Medical Center

Study Sites (1)

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