Massage Therapy and the Well-Being of Police Officers

July 31, 2017 updated by: Alanah Whiteway
This study is intend to show the positive impact that massage therapy can have on the lives of police officers. The study will demonstrate how regular treatment can change sleeping quality, stress levels and mental health. It will also investigate the impact that police work can have on the body.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

6

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 Contact

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Police Officers preferable working on the street within the St. John's area

Exclusion Criteria:

  • Civilians

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscular Imbalances
Time Frame: After 12 one hour massages
A measure of any muscular imbalances that present in each clients. All client findings will be compared to see if there is a pattern through the participants. Clients will have notes compared from the beginning to the end as well to see if there has been any improvement.
After 12 one hour massages
Postural Dysfunctions
Time Frame: After 12 one hour massages
A postural assessment will be done at the beginning of the study and then be compared to one done at the end to see if there have been any improvements. All clients postural assessments will be compared to see if there is any pattern among participants. The main focus will be on the back and hip.
After 12 one hour massages
Range of Motion
Time Frame: After 12 one hour massages
The range of motion of major joints will be assess to see if they fall within the norm, or if each client is limited. The client will have a range of motion test done at the beginning of treatment and again at the end to see if there has been any improvement. All clients range of motion testing will be compared to see if there are any patterns throughout the officers.
After 12 one hour massages

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Stress Levels
Time Frame: After 12 one hour massages
Stress levels will be rated on a scale of 1 to 5 (one being no stress and 5 being extremely stressed) to see if during the duration of the study they find a decrease in their stress levels.
After 12 one hour massages
Sleep Quality
Time Frame: After 12 one hour massages
To see if there is improvement of sleep quality in general, and sleep quality during change over shifts. Sleep will be rated on a scale of 1 to 5 (One being no sleep and five being a complete night of uninterrupted sleep). This will compared from studies completed throughout the study.
After 12 one hour massages
Mental Wellness
Time Frame: After 12 one hour massages
The clients will be asked to fill out a survey throughout the study on how the feel mental. It will be rated on a scale of 1 to 5 (one be extremely depressed and 5 being over the moon happy) These will be compared from the beginning to the end of treatment to see if there is any improvements.
After 12 one hour massages

Collaborators and Investigators

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

Sponsor

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 (Anticipated)

September 1, 2017

Primary Completion (Anticipated)

December 1, 2017

Study Completion (Anticipated)

December 1, 2017

Study Registration Dates

First Submitted

July 24, 2017

First Submitted That Met QC Criteria

July 27, 2017

First Posted (Actual)

August 1, 2017

Study Record Updates

Last Update Posted (Actual)

August 2, 2017

Last Update Submitted That Met QC Criteria

July 31, 2017

Last Verified

July 1, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • MTPO

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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