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- Essai clinique NCT07925736
ALAS PROPIAS: BMGIM for Professionals Working in Intimate Partner Machista Violence Services (ALAS PROPIAS)
ALAS PROPIAS Program. Music Therapy, Well-Being and Psychological Health in the Context of Machista Violence in Intimate Partner Relationships: A Triangulation Study
This study evaluates the impact of a 10-session individual music therapy intervention using the Bonny Method of Guided Imagery and Music (BMGIM) on the well-being and psychological health of professionals working in services supporting women experiencing intimate partner machista violence.
The study uses a controlled, non-randomized quasi-experimental design, with an experimental group and a wait-list control group. Changes in burnout, compassion fatigue, vicarious trauma, secondary traumatic stress, anxiety, positive and negative affect, emotional regulation, and professional well-being are assessed.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Professionals working in services supporting women experiencing intimate partner machista violence may experience psychological consequences associated with continued exposure to others' traumatic experiences, including burnout, compassion fatigue, vicarious trauma, and secondary traumatic stress.
This study examines the impact of an individual music therapy intervention based on the Bonny Method of Guided Imagery and Music (BMGIM), consisting of 10 individual sessions. Using a controlled, non-randomized quasi-experimental design, outcomes in the experimental group are compared with those in a wait-list control group.
Changes in vicarious trauma and secondary traumatic stress, burnout, compassion fatigue, anxiety, positive and negative affect, emotional regulation, and professional well-being are assessed. The study aims to contribute scientific evidence on the potential of BMGIM music therapy to support the well-being and psychological health of professionals working in contexts of intimate partner machista violence.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Alicante
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Elche, Alicante, Espagne, 03202
- Universidad Miguel Hernández de Elche
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Professionals working in centers or shelters supporting women experiencing intimate partner machista violence.
- Direct professional contact with cases of intimate partner violence.
- Interest in participating in the individual BMGIM intervention and provision of informed consent.
Exclusion Criteria:
- Active psychosis.
- Unstabilized suicidal crisis.
- Uncontrolled substance use that prevents participation.
- Inability to attend weekly sessions
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Individual BMGIM Music Therapy
Participants receive 10 individual music therapy sessions using the Bonny Method of Guided Imagery and Music (BMGIM). |
The ALAS PROPIAS intervention consists of 10 individual music therapy sessions using the Bonny Method of Guided Imagery and Music (BMGIM), aimed at professionals working in services supporting women experiencing machista violence in intimate partner relationship. The intervention focuses on exploring imagery, emotions, and sensations through guided music listening, followed by a process of integration and reflection. The program aims to evaluate changes in burnout, compassion fatigue, vicarious trauma, secondary traumatic stress, anxiety, positive and negative affect, emotional regulation, psychological well-being, and professional well-being among participants. |
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Aucune intervention: Control Group (Wait-List)
Participants complete the same assessments as the experimental group during the initial study period but do not receive the intervention during this phase. The intervention may be offered after the initial data collection, in accordance with the study protocol. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Burnout
Délai: Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
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Burnout will be assessed using the Spanish adaptation of the Maslach Burnout Inventory (MBI) (Maslach & Jackson, 1981; Seisdedos, 1997). Scores at the final assessment will be compared with baseline scores to evaluate changes in burnout among participants in the experimental and wait-list control groups. |
Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
|
Change in Positive and Negative Affect
Délai: Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
Positive and negative affect will be assessed using the Spanish adaptation of the Positive and Negative Affect Schedule (PANAS) (Sandín et al., 1999). Scores at the final assessment will be compared with baseline scores to evaluate changes in positive and negative affect in the experimental and wait-list control groups. |
Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
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Change in Psychological Well-Being
Délai: Psychological well-being will be assessed using the Spanish adaptation of Ryff's Psychological Well-Being Scales (Díaz et al., 2006). Scores at the final assessment will be compared with baseline scores to evaluate changes in psychological well-being in
|
Psychological well-being will be assessed using the Spanish adaptation of Ryff's Psychological Well-Being Scales (Díaz et al., 2006). Scores at the final assessment will be compared with baseline scores to evaluate changes in psychological well-being in the experimental and wait-list control groups. |
Psychological well-being will be assessed using the Spanish adaptation of Ryff's Psychological Well-Being Scales (Díaz et al., 2006). Scores at the final assessment will be compared with baseline scores to evaluate changes in psychological well-being in
|
|
Change in Professional Quality of Life
Délai: Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
Professional quality of life will be assessed using the Spanish adaptation of the Professional Quality of Life Scale, version 5 (ProQOL-5) (Galiana et al., 2020). Scores at the final assessment will be compared with baseline scores to evaluate changes in professional quality of life in the experimental and wait-list control groups. |
Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
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Change in Secondary Traumatic Stress
Délai: Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
Secondary traumatic stress will be assessed using the Secondary Traumatic Stress Scale (STSS) (Guerra & Saiz, 2007). Scores at the final assessment will be compared with baseline scores to evaluate changes in secondary traumatic stress in the experimental and wait-list control groups. |
Baseline (T0), Immediate Post-intervention (T1), 3-month Follow-up (T2)
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Eva Maria León Zarceño, Universidad Miguel Hernández de Elche.
- Chercheur principal: Vicente Alejandro March Luján, Catholic University of Valencia
- Chercheur principal: Marie Laure Rodríguez-Quiroga, Universidad Miguel Hernández de Elche.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- IDE.DEMLZ.MLRQ.24_2
- IDE.DEMLZ.MLRQ.24 (Autre identifiant: Universidad Miguel Hernández)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
De-identified individual participant data (IPD) underlying the primary and secondary outcomes will be made available to qualified researchers upon reasonable request submitted to the principal investigator. Data sharing will be subject to ethical review, a formal data-sharing agreement, and strict compliance with European Union GDPR regulations to safeguard minor participants' confidentiality.
Délai de partage IPD
Data will become available after the primary manuscript publishing the final longitudinal findings is accepted
Critères d'accès au partage IPD
Individual participant data will not be publicly shared to protect minor participants' confidentiality in compliance with GDPR and local data protection regulations. Aggregate data and protocol materials are available upon request
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- CIF
Informations sur les médicaments et les dispositifs, documents d'étude
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