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Prevention of Burnout in Spanish Healthcare Professionals Through Attachment-Based Compassion Therapy (ABCT)

7. Juli 2026 aktualisiert von: Javier Garcia Campayo, Hospital Miguel Servet

Mindfulness-based and Compassion-based Interventions in Anxious-Depressive Symptomatology in Mental Health Services: A Randomized Controlled Trial.

Burnout is a common problem among healthcare professionals and may affect their psychological well-being, quality of life, and professional functioning. This study will examine whether an intensive compassion-based intervention can help reduce burnout and improve well-being in healthcare professionals. Participants will be randomly assigned to either an Attachment-Based Compassion Therapy intervention or a relaxation intervention. Outcomes will be measured before the intervention, immediately after the intervention, and three months later.

Attachment-Based Compassion groups will be composed of 80 participants each, and TAU group will be composed of 80 participants (total sample n = 160).

Burnout Inventory-Human Services Survey - MBI-HSS. Burnout will be assessed using the Maslach Burnout Inventory-Human Services Survey. This questionnaire evaluates the three main dimensions of burnout: emotional exhaustion, depersonalization, and personal accomplishment.

Items are rated on a Likert-type scale according to the frequency with which the participant experiences each symptom. Scores are calculated separately for each burnout dimension.

In this study, emotional exhaustion and depersonalization will be considered the primary outcome variables, while reduced personal accomplishment will be considered a secondary outcome variable

Studienübersicht

Status

Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

180

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Spanien
      • Zaragoza, Spanien, 50009
        • Rekrutierung
        • Miguel Servet University Hospital
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  1. Active healthcare professionals (physicians and nurses) of both sexes.
  2. Understanding of spoken and written Spanish.
  3. Availability of a computer and internet connection.
  4. Written informed consent.

Exclusion Criteria:

  • Previous psychological treatment within the last year, or current psychological treatment.

Presence of a severe uncontrolled medical, infectious, or degenerative disease that may interfere with affective symptoms.

Presence of a mental disorder related to substance dependence/abuse, or any other disease affecting the central nervous system.

Suicide risk, defined as a score of ≥2 on item 9 of the PHQ-9. Scheduled surgical intervention during the course of the study.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Compassion condition
one weekend group sessions, held Friday evening, Saturday morning and evening and Sunday morning
Verhalten: Attachment-based compassion therapy Compassion

Program consists of 8 session of 120 minutes/session (15-20 people) Written material andsound recordings will be offered as support elements.

The estimated duration of the program is one weekend
Experimental: Relaxation condition
one weekend group sessions, held Friday evening, Saturday morning and evening and Sunday morning
Verhalten: Relaxation program

Relaxation program consists of 8 sessions of 120 minutes/session (15-20 people) Written material and sound recordings will be offered as support elements.

The estimated duration of the program is one weekend

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Baseline
In the compassion program group
Baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: baseline
In the relaxation program group
baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Baseline
In the compassion program group
Baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: baseline
In the relaxation program group
baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
MASLACH BURNOUT INVENTORY HUMAN SERVICES SURVEY (MBI-HSS)
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
Burnout Clinical Subtype Questionnaire BCSQ-12
Zeitfenster: Baseline
In the compassion program group
Baseline
Burnout Clinical Subtype Questionnaire BCSQ-12
Zeitfenster: baseline
In the relaxation program group
baseline
Burnout Clinical Subtype Questionnaire BCSQ-12
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Burnout Clinical Subtype Questionnaire BCSQ-12
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Burnout Clinical Subtype Questionnaire BCSQ-12
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
Burnout Clinical Subtype Questionnaire BCSQ-12
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
Sussex-Oxford Compassion for the Self Scale (SOCS-S)
Zeitfenster: Baseline
In the compassion program group
Baseline
Sussex-Oxford Compassion for the Self Scale (SOCS-S)
Zeitfenster: baseline
In the relaxation program group
baseline
Sussex-Oxford Compassion for the Self Scale (SOCS-S)
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Sussex-Oxford Compassion for the Self Scale (SOCS-S)
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Sussex-Oxford Compassion for the Self Scale (SOCS-S)
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
Sussex-Oxford Compassion for the Self Scale (SOCS-S)
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
Sussex-Oxford Compassion for Others Scale (SOCS-O)
Zeitfenster: Baseline
In the compassion program group
Baseline
Sussex-Oxford Compassion for Others Scale (SOCS-O)
Zeitfenster: baseline
In the relaxation program group
baseline
Sussex-Oxford Compassion for Others Scale (SOCS-O)
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Sussex-Oxford Compassion for Others Scale (SOCS-O)
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Sussex-Oxford Compassion for Others Scale (SOCS-O)
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
Sussex-Oxford Compassion for Others Scale (SOCS-O)
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
Depression Anxiety Stress Scales - DASS-21
Zeitfenster: Baseline
In the compassion program group
Baseline
Depression Anxiety Stress Scales - DASS-21
Zeitfenster: baseline
In the relaxation program group
baseline
Depression Anxiety Stress Scales - DASS-21
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Depression Anxiety Stress Scales - DASS-21
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Depression Anxiety Stress Scales - DASS-21
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
Depression Anxiety Stress Scales - DASS-21
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
FIVE FACETS MINDFULNESS QUESTIONNAIRE FFMQ
Zeitfenster: Baseline
In the compassion program group
Baseline
FIVE FACETS MINDFULNESS QUESTIONNAIRE FFMQ
Zeitfenster: baseline
In the relaxation program group
baseline
FIVE FACETS MINDFULNESS QUESTIONNAIRE FFMQ
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
FIVE FACETS MINDFULNESS QUESTIONNAIRE FFMQ
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
FIVE FACETS MINDFULNESS QUESTIONNAIRE FFMQ
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
FIVE FACETS MINDFULNESS QUESTIONNAIRE FFMQ
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
Basic Psychological Needs Satisfaction Scale - General
Zeitfenster: Baseline
In the compassion program group
Baseline
Basic Psychological Needs Satisfaction Scale - General
Zeitfenster: baseline
In the relaxation program group
baseline
Basic Psychological Needs Satisfaction Scale - General
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Basic Psychological Needs Satisfaction Scale - General
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Basic Psychological Needs Satisfaction Scale - General
Zeitfenster: Three months follow up
In the compassion program group
Three months follow up
Basic Psychological Needs Satisfaction Scale - General
Zeitfenster: Three months follow up
In the relaxation program group
Three months follow up
Treatment Received Satisfaction Scale
Zeitfenster: Baseline
In the compassion program group
Baseline
Treatment Received Satisfaction Scale
Zeitfenster: baseline
In the relaxation program group
baseline
Treatment Received Satisfaction Scale
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Treatment Received Satisfaction Scale
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Treatment Received Satisfaction Scale
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
Treatment Received Satisfaction Scale
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]
Reduced scale Highly Sensitive Person Scale to the Adult Spanish Population (RHSP)
Zeitfenster: Baseline
In the compassion program group
Baseline
Reduced scale Highly Sensitive Person Scale to the Adult Spanish Population (RHSP)
Zeitfenster: baseline
In the relaxation program group
baseline
Reduced scale Highly Sensitive Person Scale to the Adult Spanish Population (RHSP)
Zeitfenster: Post-treatment 1 weekend from baseline
In the compassion program group
Post-treatment 1 weekend from baseline
Reduced scale Highly Sensitive Person Scale to the Adult Spanish Population (RHSP)
Zeitfenster: Post-treatment 1 weekend from baseline
In the relaxation program group
Post-treatment 1 weekend from baseline
Reduced scale Highly Sensitive Person Scale to the Adult Spanish Population (RHSP)
Zeitfenster: Three-months follow-up]
In the compassion program group
Three-months follow-up]
Reduced scale Highly Sensitive Person Scale to the Adult Spanish Population (RHSP)
Zeitfenster: Three-months follow-up]
In the relaxation program group
Three-months follow-up]

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Hospital Miguel Servet

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

10. Juli 2026

Primärer Abschluss (Geschätzt)

30. November 2026

Studienabschluss (Geschätzt)

30. April 2028

Studienanmeldedaten

Zuerst eingereicht

7. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

7. Juli 2026

Zuerst gepostet (Tatsächlich)

13. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

13. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

7. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • 11/2026

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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