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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03245034
Other study ID # 16-02292
Secondary ID
Status Completed
Phase N/A
First received August 7, 2017
Last updated October 6, 2017
Start date June 1, 2017
Est. completion date September 1, 2017

Study information

Verified date October 2017
Source New York University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This feasibility study develops methods for larger-scale research, evaluating the acceptability and perceived impact of a group acupuncture and acupressure intervention, as well as suitability of a self-report instrument. During their weekly training program, eleven OB residents at NYU Lutheran Medical Center will receive three sessions of auricular acupuncture therapy. (This resident population was previously anonymously surveyed and all expressed interest in participating in such a study). The Professional Quality of Life Scale (ProQOL) will be administered at 6 time points. A brief survey will also be given to assess participants' acceptance of the intervention as well as applicability of the ProQOL instrument. Additional feasibility-related outcomes include protocol compliance/withdrawals, adverse events, and time taken to complete intervention and surveys.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date September 1, 2017
Est. primary completion date September 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 44 Years
Eligibility Inclusion Criteria:

- Enrollment in NYU Lutheran Obstetrics & Gynecology Residency program

Exclusion Criteria:

- Women currently pregnant or attempting to conceive

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Auricular Acupuncture Therapy
Acupuncture treatment will be the NADA protocol, a well-known and commonly used protocol that has previously been studied for stress relief in health care workers.In this protocol, 5, ½" needles are inserted in each auricle and retained while the group relaxes for 20 minutes. It will be conducted by two acupuncturists credentialed at NYU Lutheran (TK and AG).

Locations

Country Name City State
United States New York University School of Medicine New York New York

Sponsors (1)

Lead Sponsor Collaborator
New York University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Professional Quality of Life (ProQOL) he ProQOL is the most commonly used measure of the negative and positive affects of helping others who experience suffering and trauma. The ProQOL has sub-scales for compassion satisfaction, burnout and compassion fatigue. 4 Weeks
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