NCT02378597

Brief Summary

To develop and test a 4-session program to teach resiliency skills to Medical Interpreters.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2014

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2014

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2014

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2014

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

June 27, 2014

Completed
8 months until next milestone

First Posted

Study publicly available on registry

March 4, 2015

Completed
Last Updated

December 5, 2025

Status Verified

November 1, 2025

Enrollment Period

2 months

First QC Date

June 27, 2014

Last Update Submit

November 30, 2025

Conditions

Psychological Stress

Keywords

Resiliency burnout stress

Outcome Measures

Primary Outcomes (1)

  • Feasibility and Acceptability of Intervention (participant feedback questionnaire)

    A participant feedback questionnaire will be completed by participants, including questions about whether the logistics and content of the intervention were feasible and acceptable to them. Attendance to the sessions is also considered as a component of feasibility.

    Post-Intervention (4 weeks)

Secondary Outcomes (1)

  • Psychological Variables including Perceived Stress and Resiliency ( PSS-1021 is a 10-item scale)

    Baseline, Post-Intervention (4 weeks), and 12 week follow up

Study Arms (2)

Delayed Intervention: Control

ACTIVE COMPARATOR

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: Behavioral: Resiliency Intervention

Experimental: Intervention

EXPERIMENTAL

Experimental: Intervention was a 4 hour behavioral resiliency intervention.

Behavioral: Behavioral: Resiliency Intervention

Interventions

Behavioral: Resiliency InterventionBEHAVIORAL

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.

Also known as: CARE
Delayed Intervention: ControlExperimental: Intervention

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Interpreter employed at one of the 3 study hospitals
  • \>=20 hours/week

You may not qualify if:

  • \) Interpreter working \<20 hours per week

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Stress, Psychological

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Study Officials

  • Michele Russell-Einhorn, JD

    Dana-Farber Cancer Institute

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

June 27, 2014

First Posted

March 4, 2015

Study Start

January 1, 2014

Primary Completion

March 1, 2014

Study Completion

June 1, 2014

Last Updated

December 5, 2025

Record last verified: 2025-11