CBCT for Spiritual Health Clinicians
19 maggio 2020 aggiornato da: Jennifer Mascaro, Emory University
Exploring the Effect of Cognitively-Based Compassion Training (CBCT) on the Empathic Accuracy and Resilience of Spiritual Health Clinicians
The Emory University Spiritual Health department will incorporate Cognitively-Based Compassion Training (CBCT) into their training curriculum beginning in Fall 2017, which provides the opportunity to compare students receiving the CBCT addendum with those receiving traditional chaplaincy training.
This is a naturalistic study that examines the impact of incorporating CBCT into Emory's spiritual caregiver training program.
The researchers will examine the effect of CBCT on empathic accuracy and resilience by comparing the first group of students who receive CBCT-informed training with chaplains who receive standard training in spiritual caregiving and receive CBCT later in the residency year.
Comprehensive assessments will be conducted in order to examine whether outcomes for patients are improved for those receiving chaplain spiritual care augmented by CBCT compared to those receiving spiritual care from chaplains who receive CBCT later in their residency.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Based on a wealth of research demonstrating the associations between physical health and psychosocial well-being, modern health care in the United States is characterized by an increasingly patient-centered model of care that places a premium on the holistic treatment of the patient as a physical, psychosocial, and spiritual whole.
Hospital chaplains play a vital role in delivering emotional and spiritual care to a broad range of both religious and non-religious patients for a wide variety of stressors, and extensive research indicates that spiritual consults impact patient outcomes and satisfaction.
However, there is remarkably little research on the "active ingredients" of chaplaincy spiritual care, and a subsequent lack of standardization and best-practice guidelines informing chaplain training and chaplain spiritual consulting.
CBCT ® (Cognitively-Based Compassion Training) is a secularized compassion meditation program adapted from the Tibetan Buddhist mind training (lojong) tradition, and it may be an ideal addendum to both chaplain training programs and to the spiritual care consults provided by Emory University hospital chaplains to approximately 100,000 patients each year.
This is a pilot study to explore the feasibility and impact of incorporating CBCT into the educational curriculum for chaplain residents.
To this end, the researchers will (1) examine the impact of CBCT on burnout, compassion, and empathic accuracy among chaplains in training, (2) explore whether the impact persists through the end of the resident training, (3) evaluate the timing of the training within the existing curriculum to maximize its impact, (4) evaluate whether CBCT-informed interventions improve patient outcomes, and (5) explore chaplain and patient mediators of the impact of spiritual care consults on patient outcomes.
Data acquired in this pilot study will be used to estimate efficacy and to inform a randomized controlled trial.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
304
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Georgia
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Atlanta, Georgia, Stati Uniti, 30322
- Emory University Hospital
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Atlanta, Georgia, Stati Uniti, 30308
- Emory University Hospital Midtown
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Atlanta, Georgia, Stati Uniti, 30322
- Emory Clinic
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Atlanta, Georgia, Stati Uniti, 30322
- Emory University Winship Cancer Institute
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Atlanta, Georgia, Stati Uniti, 30342
- St. Joseph's Hospital
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Atlanta, Georgia, Stati Uniti, 30329
- Wesley Woods Center
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Johns Creek, Georgia, Stati Uniti, 30097
- Emory Johns Creek Hospital
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria for Chaplains:
- Chaplain residents with Spiritual Health at Emory Healthcare
Inclusion Criteria for Chaplains:
- Patient of Emory Healthcare
- Requested a spiritual health consultation with a hospital chaplain
Exclusion Criteria:
- None
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Ricerca sui servizi sanitari
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Early-start group for CBCT-informed training
Hospital chaplain residents receiving the Cognitively-Based Compassion Training (CBCT) education during the first unit of their year-long residency.
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Cognitively-Based Compassion Training (CBCT) is a secularized compassion meditation program adapted from the Tibetan Buddhist mind training (lojong) tradition.
Lojong practices utilize a cognitive, analytic approach to challenge one's unexamined thoughts and emotions toward other people, with the long-term goal of developing altruistic emotions and behavior towards all people.
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Comparatore attivo: Delayed-start group for CBCT-informed training
Hospital chaplain residents receiving the Cognitively-Based Compassion Training (CBCT) education midway through their year-long residency.
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Cognitively-Based Compassion Training (CBCT) is a secularized compassion meditation program adapted from the Tibetan Buddhist mind training (lojong) tradition.
Lojong practices utilize a cognitive, analytic approach to challenge one's unexamined thoughts and emotions toward other people, with the long-term goal of developing altruistic emotions and behavior towards all people.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in Depression Anxiety and Stress Scale (DASS) Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Depression Anxiety and Stress Scale (DASS) is a 42-item likert-scale measure that assesses the frequency of symptoms of depression, anxiety and stress during the past week.
Respondents indicate the degree to which they agree with each statement on a scale of 0 to 3 where 0 = does not apply to me at all and 3 = applied to me very much, or most of the time.
Total scores range from 0 to 126 and higher scores indicate increased feelings of depression, anxiety and stress.
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Baseline, Week 5, Week 24, Week 29
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Change in Mental Health Continuum Short Form (MHC-SF) Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Mental Health Continuum Short Form (MHC-SF) is a 14-item inventory assessing emotional well-being.
Participants indicate how frequently they have experienced different feelings (such as feeling happy) in the past month.
Responses are are a 6-point scale where 0 = never and 5 = every day.
Total scores range from 0 to 70 and higher scores indicate greater well being.
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Baseline, Week 5, Week 24, Week 29
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Change in Professional Quality of Life Scale (ProQOL) Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Professional Quality of Life Scale (ProQOL) is a 30-item inventory, the ProQOL is the most commonly used measure of the negative and positive effects of helping others who experience suffering.
It has sub-scales for compassion satisfaction, burnout, and compassion fatigue.
The sub-scales are summed and converted to t-scores with a mean of 50 and standard deviation of 10.
Scores higher than 57 indicate professional satisfaction while scores below 40 indicate possible problems with feeling satisfied professionally.
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Baseline, Week 5, Week 24, Week 29
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Change in School-Burnout Inventory (SBI) Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The School-Burnout Inventory is a 9-item survey asking students about how much burnout, in the context of an academic environment, they have felt in the past month (for example, "I feel overwhelmed by my schoolwork").
Respondents indicate the degree to which they agree with each statement on a scale of 1 to 6 where 1 = completely disagree and 6 = completely agree.
Total scores can range from 9 to 54, with higher scores indicating more burnout.
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Baseline, Week 5, Week 24, Week 29
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Change in Revised University of California, Los Angeles (UCLA) Loneliness Scale (R-UCLA) Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Revised UCLA Loneliness Scale (R-UCLA) is a 20-item questionnaire measuring general feelings of social isolation and dissatisfaction with one's social interactions.
Participants rate each item on a scale from 1 (never) to 4 (often).
When scoring the scale, certain items are reversed so that low scores correspond with low loneliness.
Total scores range from 20 to 80, where high scores indicate high feelings of loneliness.
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Baseline, Week 5, Week 24, Week 29
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Change in Empathic Accuracy (EA) Task Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Empathic Accuracy (EA) Task is a dynamic video assessment that asks subjects to continuously rate the emotions of others as they tell emotional autobiographical stories.
Empathic accuracy is the correlation between feelings of the story-tellers in the video and what the participants perceive the story-tellers feelings to be.
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Baseline, Week 5, Week 24, Week 29
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Change in Spiritual Meaning Scale (SMS) Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Spiritual Meaning Scale (SMS) is a 15-item, likert-scale inventory that assesses the extent to which someone endorses a belief in something larger than themselves.
Participants respond to statements like "life is inherently meaningful" on a scale of 1 to 5 where 1 = I totally disagree, 3 = I'm in between, and 5 = I totally agree.
Certain items are scored in reverse.
The total score ranges from 15 to 75 and higher scores indicate stronger belief.
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Baseline, Week 5, Week 24, Week 29
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Change in Jefferson Scale of Empathy Score
Lasso di tempo: Baseline, Week 5, Week 24, Week 29
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The Jefferson Scale of Empathy is a 20-item scale designed to measure empathy in practicing health care professionals and health care professional students.
Participants answer on a 7-point scale where 1 = strongly disagree and 7 = strongly agree.
Total scores range from 20 to 140 where higher scores indicate increased empathy.
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Baseline, Week 5, Week 24, Week 29
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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National Comprehensive Cancer Network (NCCN) Distress Thermometer
Lasso di tempo: Day 1 (before Spiritual Health consult)
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Patients will use the NCCN Distress Thermometer to rate levels of distress over the past week including the current day.
The NCCN Distress Thermometer is a single-item screener of distress, with a scale from 0 (no distress) to 10 (extreme distress) represented through a visual graphic of a thermometer.
Patients will complete the screening prior to having a Spiritual Health consult with the chaplain.
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Day 1 (before Spiritual Health consult)
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Patient-Reported Outcomes Measurement Information System (PROMIS) Self-Efficacy for Managing Emotions
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The PROMIS Self-Efficacy for Managing Emotions is a 15-item Likert scale self-report measure ("not at all confident"; "a little confident"; "somewhat confident"; "quite confident" and "very confident") completed by patients, which asks them to reflect on their own confidence levels in managing and controlling symptoms of anxiety, depression, helplessness, discouragement, frustration, disappointment, and anger.
Raw scores range from 15 to 75 with higher scores indicating increased self efficacy.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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PROMIS Positive Affect
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The PROMIS Positive Affect questionnaire is a 15-item Likert-scale self-report measure completed by patients, which assesses momentary positive or rewarding affective experiences such as feelings and moods associated with pleasure, joy, elation, contentment, pride, affection, happiness, engagement, and excitement.
Raw scores range from 15 to 75 with higher scores indicating increased positive feelings.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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Hospital Anxiety and Depression Scale (HADS)
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The Hospital Anxiety and Depression Scale (HADS) is a 14-item self-report questionnaire used to screen for the presence of depression and anxiety in physically ill patients.
It is divided into two subscales: Anxiety (HADS-A) and Depression (HADS-D).
Patients rate each item on a 4-point scale from 0 (absence) to 3 (extreme presence), with five of the 14 items reverse coded.
Total scores range from 0 to 42, with higher scores indicating greater levels of anxiety and depression.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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PROMIS Emotional Support
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The PROMIS Emotional Support is a 4-item Likert-scale that assesses perceived feelings of being cared for and valued as a person.
Each of the 4 questions has five response options ranging in value from one to five, with total scores ranging from 4 to 20.
Higher scores indicate increased feelings of being supported emotionally.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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PROMIS Informational Support
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The PROMIS Informational Support is a 4-item Likert-scale that assesses perceived availability of helpful information or advice.
Each of the 4 questions has five response options ranging in value from one to five, with total scores ranging from 4 to 20.
Higher scores indicate increased perception of available information.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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PROMIS Social Isolation
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The PROMIS Social Isolation is a 4-item Likert-scale that assesses perceptions of being avoided, excluded, detached, disconnected from, or unknown by, others.
Each of the 4 questions has five response options ranging in value from one to five, with total scores ranging from 4 to 20.
Higher scores indicate increased social isolation.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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Scottish Patient Reported Outcome Measure (PROM)
Lasso di tempo: Day 1 (after Spiritual Health consult)
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The Scottish Patient Reported Outcome Measure (PROM) is an 18-item self-report Likert-scale that assesses how a hospitalized patient perceived the Spiritual Care visit both during and after the consult.
It also assesses the patient's present state regarding their situation and whether they view themselves as a spiritual or religious person.
Responses range in value from 1 (not at all) to 5 (all of the time).
Total scores range from 18 to 90 with higher scores suggesting increased positive feelings about the spiritual care received.
Patients will complete the questionnaire after having a Spiritual Health consult with the chaplain.
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Day 1 (after Spiritual Health consult)
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
5 luglio 2018
Completamento primario (Effettivo)
7 maggio 2020
Completamento dello studio (Effettivo)
7 maggio 2020
Date di iscrizione allo studio
Primo inviato
8 maggio 2018
Primo inviato che soddisfa i criteri di controllo qualità
8 maggio 2018
Primo Inserito (Effettivo)
18 maggio 2018
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
21 maggio 2020
Ultimo aggiornamento inviato che soddisfa i criteri QC
19 maggio 2020
Ultimo verificato
1 maggio 2020
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- IRB00098222
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .