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

December 20, 2019 updated by: Aiesha Ahmed, Milton S. Hershey Medical Center
This research is being done to explore the potential benefit of a physical therapist-guided stretching program on musculoskeletal pain and well-being.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Hershey, Pennsylvania, United States, 17033
        • Penn State Health Milton S. Hershey Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1: In-Person

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.

Head/neck stretches

  • Head tilt side to side
  • Cross-chest stretch Torso stretches
  • Side stretch
  • Mid-back stretch Lower limb
  • Standing quadriceps stretch
  • Standing hamstring stretch
Experimental: Group 2: Video

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.

Head/neck stretches

  • Head tilt side to side
  • Cross-chest stretch Torso stretches
  • Side stretch
  • Mid-back stretch Lower limb
  • Standing quadriceps stretch
  • Standing hamstring stretch

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
change from 3 month time point to 6 month time point
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.
change from 3 month time point to 6 month time point

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Modified Sit and Reach
Time Frame: baseline, 3 months, 6 months, change from 3 month time point to 6 month time point
The sit and reach test is a common measure of flexibility, and specifically measures the flexibility of the lower back and hamstring muscles.
baseline, 3 months, 6 months, change from 3 month time point to 6 month time point
SF-36
Time Frame: baseline, 3 months
The 36-Item Short Form Health Survey (SF-36) is a set of generic, coherent, and easily administered quality-of-life measures.
baseline, 3 months
CMDQ
Time Frame: baseline, 3 months
The Cornell Musculoskeletal Discomfort Questionnaires (CMDQ) is a questionnaire based on previous published research studies of musculoskeletal discomfort among office workers.
baseline, 3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Aiesha Ahmed, MD, Penn State Health Milton S. Hershey Medical Center
  • Principal Investigator: Majid Dadgar-Kiani, MD, Milton S. Hershey Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 11, 2019

Primary Completion (Actual)

September 10, 2019

Study Completion (Actual)

September 10, 2019

Study Registration Dates

First Submitted

February 4, 2019

First Submitted That Met QC Criteria

February 4, 2019

First Posted (Actual)

February 6, 2019

Study Record Updates

Last Update Posted (Actual)

December 24, 2019

Last Update Submitted That Met QC Criteria

December 20, 2019

Last Verified

December 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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