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Clinical Trials/NCT02540473
NCT02540473CompletedNot Applicable

Fostering Resilience: An Intervention for Women Physicians at Risk for Burnout

Mayo Clinic1 site in 1 country44 target enrollmentStarted: February 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
44
Locations
1
Primary Endpoint
level of depression

Study Overview

Brief Summary

Physicians in general are at risk for burnout, and this risk is heightened among women, particularly mothers. In a randomized design, central hypotheses in this study are that mothers who attend our 12-week Relational Psychotherapy Mothers Group (RPMG) intervention will show significantly greater decreases in stress, depression, burnout, and associated risk biomarker indices, as compared to comparison controls (who would meet in unstructured gatherings, for an hour a week for 12 weeks). Additionally the investigators hypothesize that the gains would be maintained three months after the intervention is completed.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
25 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Inclusion of Women and Minorities:
  • •This study will be restricted to women physician mothers, who are the target of the manualized RPMG program.
  • •The study will not use race or ethnicity as a basis for selecting subjects.
  • •Inclusion of Children:
  • •This study does not include children.

Exclusion Criteria

  • •Participation in this study is open to all Mayo physician mothers with a child under the age of 18 years.
  • •As in past RPMG trials, the only exclusion criteria are if mothers were to indicate active suicidality, or meet criteria for psychoses, during initial assessments or during participation in this study.

Arms & Interventions

Group therapy

Experimental

12 week manualized group therapy (one hour per week)

Intervention: Manualized Therapy (Behavioral)

Control Group

Other

Participants get one hour of time away from patient care/duties to do as they wish.

Intervention: Control Group (Behavioral)

Outcomes

Primary Outcomes

level of depression

Time Frame: Baseline to 3 months

Beck Depression Inventory

Secondary Outcomes

  • biomarker of stress(Baseline to 3 months)
  • Parenting stress(Baseline to 3 months)
  • Professional functioning(Baseline to 3 months)
  • perceived social support(Baseline to 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Cynthia M. Stonnington, M.D.

Associate Professor of Psychiatry

Mayo Clinic

Study Sites (1)

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