Measuring the Effect of Therapeutic Massage on Pain and Discomfort in Cardiac Cath Lab Staff
Stress, Fatigue, Anxiety
About this trial
This is an interventional treatment trial for Stress focused on measuring Massage, Relaxation
Eligibility Criteria
Inclusion Criteria:
Diagnostic and interventional cardiology staff including:
- cardiologists
- cardiology fellows
- nurses
- technical staff
- and a core group of CRNA's employed by the Cardiac Catheterization Laboratory.
These staff members, per their job descriptions, wear lead aprons while caring for patients during the weeks of the massage therapy pilot study.
Exclusion Criteria:
- Individuals that decline to participate in the study.
- Massage therapy has contraindications that require a physician's order before the therapist is allowed to see the person for massage. The following total contraindications will be total exclusions for this study unless the individual gains a physician's order that negates the exclusions or defines it to a local contraindication.
Total Contraindications
- Acute sprain with swelling
- Lymphatic cancer
- Fever
Local Contraindications do not exclude the person from the study. These are area exclusions that disallow the therapist to work on a specific part of the body and/or the therapist needs to adjust techniques. The therapist will track all local contraindications.
Local contraindications:
- Varicose veins
- Pregnancy
- Trapped or pinched nerve (radicular symptoms)
- Skin abrasions, open wounds
- Venous thrombus
- Melanoma
Sites / Locations
- Mayo Clinic
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
No Intervention
10 Massages
5 Massages
Control Group
This group consists of individuals that wear lead aprons, and they will receive ten, 30-minute scheduled massage appointments during the hours the participant is working in the cardiac lab, over a 10 week period.
This group consists of individuals that wear lead aprons, and they will receive five, 30-minute scheduled massage appointments, during the hours the participant is working in the cardiac lab, over a 5 week period. This arm will not receive massages for the first 5 weeks and then will receive their massages during the second 5 week period.
This group will consist of those individuals that wear lead aprons with no desire to participate in the massage study yet are willing to provide information through questionnaires. They will be given the same questionnaire as those in the two massage therapy arms of the study, at the beginning, middle, and end of study.