Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
28 participants
INTERVENTIONAL
2014-01-31
2014-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Delayed Intervention: Control
Delayed intervention: Control was a a behavioral treatment for resiliency delivered in a single 4 hour session delivered in a delayed fashion (waitlist control)
Behavioral: Resiliency Intervention
4 hour behavioral session including education in the relaxation response, education about stress and allostatic load, cognitive skills building, review of difficult encounters with patients.
Experimental: Intervention
Experimental: Intervention was a 4 hour behavioral resiliency intervention.
Behavioral: Resiliency Intervention
4 hour behavioral session including education in the relaxation response, education about stress and allostatic load, cognitive skills building, review of difficult encounters with patients.
Interventions
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Behavioral: Resiliency Intervention
4 hour behavioral session including education in the relaxation response, education about stress and allostatic load, cognitive skills building, review of difficult encounters with patients.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. \>=20 hours/week
Exclusion Criteria
18 Years
80 Years
ALL
No
Sponsors
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University of Massachusetts, Boston
OTHER
Massachusetts General Hospital
OTHER
Responsible Party
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Elyse Park, PhD
Associate Professor
Principal Investigators
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Michele Russell-Einhorn, JD
Role: STUDY_DIRECTOR
Dana-Farber Cancer Institute
Other Identifiers
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12-524
Identifier Type: -
Identifier Source: org_study_id
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