Measuring the Effect of Chair Massage on Stress Related Symptoms for Nurses

Sponsor
Mayo Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT01504763
Collaborator
(none)
40
1
1
2
20

Study Details

Study Description

Brief Summary

The purpose of this study was to assess the feasibility and effect of chair massage provided during working hours for nurses in an inpatient psychiatric and an outpatient pain rehabilitation unit and on the nurses stress related symptoms.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Chair massage
N/A

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 Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Measuring the Effect of Chair Massage on Stress Related Symptoms for Nurses: A Pilot Study
Study Start Date :
Oct 1, 2010
Actual Primary Completion Date :
Dec 1, 2010
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Massage

Chair massage for 15 minutes once a week for 10 weeks.

Procedure: Chair massage
Chair massage for 15 minutes once a week for 10 weeks.
Other Names:
  • Massage
  • Outcome Measures

    Primary Outcome Measures

    1. Change in stress, anxiety and quality of life after 10 weeks of chair massage therapy in nursing staff using four self reported instruments. [10 Weeks]

    Secondary Outcome Measures

    1. Change from baseline of stress related symptoms in nursing staff at 5 weeks. [5 Weeks]

    2. Change from baseline of stress related symptoms in nursing staff at 10 weeks. [10 Weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mayo Clinic Rochester Minnesota United States 55905

    Sponsors and Collaborators

    • Mayo Clinic

    Investigators

    • Principal Investigator: Deborah J. Engen, O.T., Mayo Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Deborah Engen, Principal Investigator, Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT01504763
    Other Study ID Numbers:
    • 08-004874
    First Posted:
    Jan 5, 2012
    Last Update Posted:
    Feb 8, 2012
    Last Verified:
    Feb 1, 2012
    Keywords provided by Deborah Engen, Principal Investigator, Mayo Clinic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 8, 2012