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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01786499
Other study ID # 3888-2
Secondary ID
Status Withdrawn
Phase N/A
First received February 5, 2013
Last updated November 30, 2016
Start date June 2013

Study information

Verified date November 2016
Source Allina Health System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Hypothesis: Relaxation Response training is an effective intervention in reducing the prevalence and severity of burnout and its components from baseline levels among physicians receiving the training intervention. The intervention is hypothesized to moderate the relationship between Areas of Worklife (AWS) and burnout by improving physician's ability to cope with the demands of their workplace. This increased coping ability is hypothesized to reduce burnout.

Physician practices are as unique as the individual practitioners and the environment in which they practice. Traditional instruction of relaxation or self-care techniques has required participants to travel to locations remote from the workplace. The time commitment required for this behavior is additive to the time required to learn the intervention and of itself may induce extra stress increasing the potential for burnout. This study proposes that bringing the intervention to the workplace will increase provider willingness to participate and diminish the stress introduced by deployment of the intervention. Since inpatient and outpatient medicine have different practice characteristics and demands on the time of the practitioners, this study will need to develop and test the logistics necessary to bring the training to the different physician populations.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date December 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Providers at designated clinic and hospital

Exclusion Criteria:

Study Design

Intervention Model: Single Group Assignment, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Relaxation Response Training


Locations

Country Name City State
United States Allina Health Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Allina Health System

Country where clinical trial is conducted

United States, 

References & Publications (2)

Benson H, Greenwood MM, Klemchuk H. The relaxation response: psychophysiologic aspects and clinical applications. Int J Psychiatry Med. 1975;6(1-2):87-98. — View Citation

Leiter, M. P., & Maslach, C. (2004). Areas of worklife: A structured approach to organizational predictors of job burnout. Research in Occupational Stress and Well being: Emotional and Physiological Processes and Positive Intervention Strategies, 3, 92-134.

Outcome

Type Measure Description Time frame Safety issue
Primary Change in burnout expression in study population Measurement strategy: data collection at Baseline (prior to beginning of the Relaxation Response training), 3 months, 6 months, 12 months, 18 months, and 24 months after implementation.
Measurement instruments: survey that measures prevalence and severity of burnout (Maslach Burnout Inventory, MBI), the proximate drivers of burnout (Areas of Worklife Survey), an assessment of the perceived stress experienced by the practitioners (Perceived Stress Scale), and a measure of the personal resilience (Conor-Davidson Resilience Scale). Standard univariate statistics will be used to produce descriptive measures of the sample, Chronbach's alpha to assess internal reliability of survey measures, and confirmatory factor analysis will be employed to determine if the data fits the a priori theoretical model. A combination of the approaches above will help to assess the effectiveness of the Relaxation Response intervention on the prevalence, incidence, and trajectory of provider burnout.
Three months No
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