NCT03212417

Brief Summary

The purpose of this study is to evaluate the impact education has on reducing compassion fatigue in Oncology Clinical Research Nurses.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2017

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

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

June 6, 2017

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

June 29, 2017

Completed
12 days until next milestone

First Posted

Study publicly available on registry

July 11, 2017

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 17, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 17, 2019

Completed
Last Updated

October 3, 2019

Status Verified

October 1, 2019

Enrollment Period

2.1 years

First QC Date

June 29, 2017

Last Update Submit

October 2, 2019

Conditions

Normal Volunteer

Outcome Measures

Primary Outcomes (2)

  • Participation in intervention (Yes/No)

    Two months post intervention

  • Participation in intervention and ProQoL survey (Professional Quality of Life: Compassion and Satisfaction Fatigue Version 5) at one-month and two-month assessment (Yes/No) Coping Mechanisms survey.

    Three months post intervention

Secondary Outcomes (5)

  • Descriptive analysis on participant's data collected by demographic information form, including

    Three months post intervention

  • Descriptive analysis (median and range) on participant's ProQol score collected by ProQol survey (Professional Quality of Life: Compassion and Satisfaction Fatigue Version 5) at the intervention, one-month, and two-month assessment.

    From intervention to two-month post intervention

  • Calculate the changes of ProQol score from intervention to one-month post intervention

    From intervention to one-month post intervention

  • Calculate the changes of ProQol score from intervention to two-month post intervention

    From intervention to two-month post intervention

  • Descriptive analysis (median and range) on participant's coping mechanisms score collected at the three-month post intervention

    From intervention to three-month post intervention

Study Arms (1)

Interventional trial without phases-supportive care.

OTHER

This is a feasibility pilot study project assessing the presence of compassion fatigue in clinical research nurses (cohort 1) and bone marrow transplant nurses (cohort 2). A survey will be completed by participants prior to and after an educational presentation. The intervention includes the risk factors, signs and symptoms, and interventions on compassion fatigue. The survey will be completed prior to the education, immediately following the education, one month following the education and two months following the education. A final survey will be implemented for the cohort 2 only. The objective of this concluding analysis is to gather data relative to CF and coping mechanisms.

Other: Educational intervention

Interventions

Educational interventionOTHER

Presentation of risk factors, signs and symptoms, and interventions on compassion fatigue

Interventional trial without phases-supportive care.

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Documented written informed consent of participant
  • Must be a Clinical Research Nurse working in the Clinical Trials Office or a Bone Marrow Transplant nurse working at COH National Medical Center
  • Ability read and speak English, (questionnaires are in English)
  • Willingness and ability to complete three ProQol 5 surveys, one demographic survey,and Coping Mechanisms survey (cohort 2).
  • Willingness to participate in a 30-minute educational intervention.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

City of Hope Medical Center

Duarte, California, 91010, United States

Location

MeSH Terms

Interventions

Early Intervention, Educational

Intervention Hierarchy (Ancestors)

Child Health ServicesCommunity Health ServicesHealth ServicesHealth Care Facilities Workforce and ServicesPreventive Health Services

Study Officials

  • Lynette Svingen, MBA/MHA, RN, BSN

    City of Hope Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 29, 2017

First Posted

July 11, 2017

Study Start

June 6, 2017

Primary Completion

July 17, 2019

Study Completion

July 17, 2019

Last Updated

October 3, 2019

Record last verified: 2019-10

Data Sharing

IPD Sharing
Will not share

Locations

US(1)