- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03831737
Team-based Ergonomics Educational Model for Workplace WELLNESS Improvement: A Pilot Study (TEEM WELLNESS)
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Hershey, Pennsylvania, United States, 17033
- Penn State Health Milton S. Hershey Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
|
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
|
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
Sponsor
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
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11328 (DAIDS ES)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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