- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01504763
Measuring the Effect of Chair Massage on Stress Related Symptoms for Nurses
Measuring the Effect of Chair Massage on Stress Related Symptoms for Nurses: A Pilot Study
Study Overview
Status
Intervention / Treatment
Detailed Description
Nursing staff working in a hospital in-patient psychiatric unit and out-patient pain rehabilitation/ fibromyalgia units each have varying causes of stress as both are intensely demanding environments. The physical and psychosocial demands of these stress-loaded work environments place a significant amount of strain on the physiological well-being of the employee.
Nurses in these settings are considered healthy employees and able to participate in the workforce, although symptoms such as headaches, shoulder tension, insomnia, fatigue, and muscle and joint pain are often a part of their work day. As these stress related symptoms become more chronic, they lead to days missed and become pre-cursors to physiological illnesses so warrant further search for prevention tactics.
Massage therapy has been noted to decrease levels of anxiety and fatigue which is essential to maintaining employee's efficient care in a dynamic environment. This study will provide massage in the workplace utilizing chair massage as it is easy to set up, does not need a great deal of space, and can be provided in semi-private areas, as the participant remains clothed. A 2006 report on a small study indicated chair massage can be effective in reducing stress perception in nurses within a hospital setting, at least in the short-term. Another study reported some short-term positive effects on stress related symptoms; and came to the conclusion that further studies are indicated to examine the efficacy of workplace-based massage therapy programs.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minnesota
-
Rochester, Minnesota, United States, 55905
- Mayo Clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Men and women age 18-65 able to give informed consent
- Able to speak and understand English
- Minimum of 8-hour per day shift schedule with .75 - 1.0 FTE.
- Need to be able to schedule one massage per week in the available massage schedule time slots.
Exclusion Criteria:
- Individuals being treated for acute musculoskeletal symptoms
- Individuals currently on work restrictions
- Undergoing treatments for a malignancy
- Pregnancy (due to this being chair massage)
- Recent head, neck, shoulder or back surgeries
- Pins or joint fusion of the head or neck
- Current sinus infections, earaches, or vascular migraines
- Nursing staff that float on to the unit
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Massage
Chair massage for 15 minutes once a week for 10 weeks.
|
Chair massage for 15 minutes once a week for 10 weeks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in stress, anxiety and quality of life after 10 weeks of chair massage therapy in nursing staff using four self reported instruments.
Time Frame: 10 Weeks
|
10 Weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change from baseline of stress related symptoms in nursing staff at 5 weeks.
Time Frame: 5 Weeks
|
5 Weeks
|
Change from baseline of stress related symptoms in nursing staff at 10 weeks.
Time Frame: 10 Weeks
|
10 Weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Deborah J. Engen, O.T., Mayo Clinic
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 08-004874
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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