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CompletedNCT03286192Updated Aug 6, 2018

Compassion Cultivation Training for Nurses

An interventional study of compassion cultivation training in Feasibility, sponsored by University of Miami. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-08-06.

Sponsored by University of Miami · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate the feasibility of implementing a Compassion Cultivation Training (CCT) program for oncology nurses at Sylvester Comprehensive Cancer Center. The goal of CCT is to provide a structured and systematic way of cultivating daily-life skills needed to strengthen qualities of compassion, empathy, and kindness for oneself and others. CCT typically includes (i) eight weekly 2-hour classes and (ii) daily practice. The in-class activities include pedagogical instruction and active group discussion, guided meditation, interactive practical exercises, and sharing of inspiring readings/stories to prime feelings of open-heartedness or connection to others.

Read the detailed description

The Compassion Cultivation Training (CCT) protocol is a secular course that was developed by the Center for Compassion \& Altruism Research and Education (CCARE) at Stanford University, School of Medicine (Jinpa, 2013). The course was developed by Thupten Jinpa, PhD, in collaboration with contemplative scholars, psychologists, and scientist at Stanford. The goal of CCT is to provide a structured and systematic way of cultivating daily-life skills needed to strengthen qualities of compassion, empathy, and kindness for oneself and others. CCT typically includes (i) eight weekly 2-hour classes and (ii) daily practice. The in-class activities include pedagogical instruction and active group discussion, guided meditation, interactive practical exercises, and sharing of inspiring readings/stories to prime feelings of open-heartedness or connection to others. The daily practice includes both formal and informal practices. Participants are provided with formal guided meditations that are 15 to 30 minutes long in the form of MP3 or cds. Participants may receive practices and instructions via email with a link to the location of the MP3. They will be provided with practice logs to report their amount of practice as well as some basic observations to the research team. In the present study, we will follow the official CCT manual. The training is composed of 8 sessions, which can be delivered in 7-10 weeks.

02

Conditions studied

  • Feasibility
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Be 18 years of age or older
  2. Be willing and able to give informed consent
  3. Be a Registered Nurse (RN)
  4. Currently works at Sylvester Comprehensive Cancer Center
  5. Currently works at least 20 hours/week
  6. Be able to speak and read English

Exclusion criteria

Exclusion Criteria:

  1. Any participants who are deemed to present an acute safety risk to self or others.
  2. Any infants, children, or teenagers under 18 years of age.
  3. Prisoners
04

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    Single-Arm Intervention

    All participants in this arm receive compassion cultivation training

    Behavioral: compassion cultivation training

Interventions

  • Behavioralcompassion cultivation training

    Eight 2-hour group sessions that provide a structured and systematic way of cultivating daily-life skills needed to strengthen qualities of compassion, empathy, and kindness for oneself and others.

05

What researchers measure

Primary outcomes

  1. Number of individuals who do not drop out of the study prior to completing the post-intervention assessment

    Number of individuals who do not drop out of the study prior to completing the post-intervention assessment

    Time frame: 24 weeks after first session

Secondary outcomes

  1. Perceived Stress Scale

    self-report instrument that measures perceptions of stress

    Time frame: baseline and 7-10 weeks

  2. Maslach Burnout Inventory

    self-report instrument that measures emotional exhaustion, depersonalization, and acheivement

    Time frame: baseline and 7-10 weeks

  3. Philadelphia Mindfulness Scale

    self-report instrument that measures present moment awareness and acceptance

    Time frame: baseline and 7-10 weeks

  4. Distress Tolerance Scale

    self-report instrument that measures feelings of distress

    Time frame: baseline and 7-10 weeks

  5. SF-36

    self-report measure of health-related quality of life

    Time frame: baseline and 7-10 weeks

06

Study locations

1 site
  • Sylvester Comprehensive Cancer Center
    Miami, Florida 33136, United States
07

References and documents

Study documents

  • Informed consent form · Aug 10, 2017
  • Protocol and statistical analysis plan · Aug 10, 2017

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT03286192
Lead sponsor
University of Miami
Responsible party
Debbie Anglade (Assistant Professor, University of Miami) — Principal investigator
First posted
Sep 18, 2017
Start date
Sep 27, 2017
Primary completion
Aug 2, 2018
Completion
Aug 2, 2018
Last update
Aug 6, 2018

Study contacts

Debbie Anglade, PhD
principal investigator · University of Miami

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

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