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Trauma-Informed Education and Self-Care for Social Work Students During Field Practicum (TIESC)

28 de septiembre de 2026 actualizado por: Hakan Baydur, Manisa Celal Bayar University

Effectiveness of a Trauma-Informed Education and Self-Care Intervention in Undergraduate Social Work Students: A Protective Intervention Study Against Secondary Traumatic Stress

This study aims to evaluate the effectiveness of a structured Trauma-Informed Education and Self-Care Intervention in reducing secondary traumatic stress among undergraduate social work students completing their field practicum.

During field education, social work students may have direct professional contact with individuals affected by child abuse and neglect, domestic violence, poverty, loss, and other potentially traumatic experiences. Repeated indirect exposure to clients' traumatic experiences may place students at risk for secondary traumatic stress.

A total of 80 fourth-year undergraduate social work students will participate in the study. Participants will be allocated to an intervention group (n=40) or a control group (n=40) according to the geographic location of their routine field practicum. Students completing their field practicum in Manisa Province will constitute the intervention group, whereas students completing their field practicum outside Manisa Province, including İzmir and other provinces, will constitute the control group.

The intervention group will receive a two-hour Trauma-Informed Education and Self-Care workshop before or at the beginning of field practicum, followed by three structured self-help and peer-sharing group sessions during the practicum period. The control group will continue the routine field practicum process and standard university internship orientation without receiving the study-specific intervention during the study period.

Secondary traumatic stress will be assessed repeatedly in both groups throughout the approximately four-month practicum period. Psychological resilience will be assessed at baseline as a supportive participant characteristic. Intervention-related knowledge and skills will also be assessed in the intervention group.

The primary hypothesis is that students participating in the Trauma-Informed Education and Self-Care Intervention will demonstrate a more favorable change in secondary traumatic stress over time compared with students in the control group.

Descripción general del estudio

Descripción detallada

This prospective, non-randomized, parallel-group, quasi-experimental controlled study will be conducted among fourth-year undergraduate students enrolled in the Department of Social Work, Faculty of Health Sciences, Manisa Celal Bayar University, during the Fall Semester of the 2026-2027 academic year.

Participants will not be individually randomized. Group allocation will be based on the geographic location of the students' routine field practicum assignments. Students completing their practicum in institutions located in Manisa Province will constitute the intervention group, while students completing their practicum in İzmir or other provinces outside Manisa will constitute the control group. This geographical separation is intended to reduce contamination between intervention and control participants.

The study will include 80 participants, with 40 participants in each study arm.

Before beginning regular client contact in the field, baseline data will be collected using a sociodemographic information form, the Secondary Traumatic Stress Scale, the Resilience Evaluation Scale, and, where applicable, the Trauma-Informed Education and Self-Care Intervention Module Knowledge and Skills Assessment Form.

Following baseline assessment, participants in the intervention group will receive a two-hour interactive Trauma-Informed Education and Self-Care workshop. The workshop will address the nature and indirect effects of trauma, recognition of physiological and emotional stress responses, coping with professional stress, breathing and grounding techniques, cognitive flexibility, professional boundaries, and self-care strategies.

After students begin direct professional contact with clients, approximately during the fourth week of practicum, secondary traumatic stress will be reassessed in both groups. Following this assessment, the intervention group will participate in the first structured Self-Help and Peer-Sharing Group session.

Two additional structured group sessions will be conducted during the remainder of the practicum period. These sessions will provide a facilitated and psychologically safe environment in which students can reflect on emotionally challenging field experiences, discuss the impact of difficult cases, review coping and self-care practices, receive peer support, and strengthen strategies for managing indirect exposure to trauma.

Data collection will take place at four main time points: baseline during the orientation period before or at the beginning of field practicum; approximately four weeks after the beginning of client contact; toward the end of November; and at the end of the practicum period in mid-December.

The control group will continue the standard field practicum and routine academic internship orientation and will not receive the study-specific Trauma-Informed Education and Self-Care Intervention or structured peer-support sessions during the evaluation period.

After completion of study assessments, participants in the control group may, upon request, receive the educational module and the Trauma-Informed Self-Care Guide.

The primary effectiveness analysis will focus on differences in changes in secondary traumatic stress over time between the intervention and control groups, particularly the group-by-time interaction.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

80

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Hakan Baydur, Prof.Dr.
  • Número de teléfono: 05067021872
  • Correo electrónico: hakan.baydur@gmail.com

Ubicaciones de estudio

      • Manisa, Turquía (Türkiye), 45020
        • Manisa Celal Bayar University Faculty of Health Sciences Department of Social Work Manisa, Türkiye
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

20 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Fourth-year undergraduate student enrolled in the Department of Social Work, Faculty of Health Sciences, Manisa Celal Bayar University, during the Fall Semester of the 2026-2027 academic year
  • Enrolled in the required Social Work Practice course
  • Actively completing a field practicum involving direct professional contact with social work clients
  • Willing to participate in the study and able to provide written informed consent

Exclusion Criteria:

  • Not actively participating in the required field practicum at the time of enrollment
  • No direct professional contact with social work clients during the practicum
  • Declining or being unable to provide written informed consent

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Trauma-Informed Education and Self-Care Intervention

Participants in this arm will receive the standard university internship orientation and routine field practicum activities in addition to two study-specific behavioral interventions: a 2-hour Trauma-Informed Education and Self-Care Psychoeducational Workshop and three structured 60-minute Self-Help and Peer-Sharing Group Sessions conducted during the field practicum.

Participants in the intervention arm will receive a 2-hour interactive psychoeducational workshop before or at the beginning of field practicum. The workshop covers trauma-informed practice, the nature and indirect effects of trauma, recognition of physiological and emotional stress responses, secondary traumatic stress, stress-management strategies, breathing and grounding exercises, cognitive flexibility, professional boundaries, and self-care strategies.

Participants in the intervention arm will participate in three structured 60-minute small-group sessions conducted during the field practicum. The sessions provide a facilitated and psychologically safe environment in which participants can reflect on emotionally challenging field experiences, discuss the emotional impact of difficult cases, receive peer support, review self-care practices, and reinforce coping and emotional regulation strategies.

Sin intervención: Standard Field Practicum and Internship Orientation

Participants in this arm will continue their routine field practicum and receive the standard academic internship orientation provided by the university. They will not receive either of the study-specific behavioral interventions during the study evaluation period. After completion of all study assessments, participants may receive the educational module and a digital Trauma-Informed Self-Care Guide upon request.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Secondary Traumatic Stress Scale Total Score
Periodo de tiempo: Baseline and Weeks 4, 8, and 12 after the start of field practicum

Secondary traumatic stress will be assessed using the 17-item Secondary Traumatic Stress Scale. Each item is rated on a five-point Likert scale. Total scores range from 17 to 85, with higher scores indicating greater secondary traumatic stress and therefore a worse outcome.

The scale will be administered at baseline and at three follow-up assessments during the field practicum. The primary outcome will be the change in Secondary Traumatic Stress Scale total scores over time and the difference in this change between the intervention and control groups.

Baseline and Weeks 4, 8, and 12 after the start of field practicum

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change From Baseline in Resilience Evaluation Scale Total Score
Periodo de tiempo: Baseline and Weeks 4, 8, and 12 after the start of field practicum

Psychological resilience will be assessed using the 9-item Turkish version of the Resilience Evaluation Scale. Total scores range from 0 to 36, with higher scores indicating greater psychological resilience and therefore a better outcome.

The scale will be administered at baseline and at three follow-up assessments during the field practicum. Changes in Resilience Evaluation Scale total scores over time will be compared between the intervention and control groups.

Baseline and Weeks 4, 8, and 12 after the start of field practicum

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Trauma-Informed Education and Self-Care Intervention Module Knowledge and Skills Assessment Form Total Score
Periodo de tiempo: Immediately after completion of the initial 2-hour training session (Day 0)

Trauma-informed education and self-care-related knowledge and skills will be assessed using the researcher-developed Trauma-Informed Education and Self-Care Intervention Module Knowledge and Skills Assessment Form.

Total scores range from 10 to 50, with higher scores indicating greater knowledge and skills related to trauma-informed practice, recognition of secondary traumatic stress, coping strategies, and self-care, and therefore a better outcome.

This assessment will be administered only to participants in the intervention group immediately after completion of the initial two-hour Trauma-Informed Education and Self-Care training session. The measure is intended to assess participants' knowledge and skill acquisition following the initial educational intervention.

Immediately after completion of the initial 2-hour training session (Day 0)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Hakan Baydur, Manisa Celal Bayar Üniversitesi

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

25 de septiembre de 2026

Finalización primaria (Estimado)

20 de enero de 2027

Finalización del estudio (Estimado)

30 de enero de 2027

Fechas de registro del estudio

Enviado por primera vez

16 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

21 de septiembre de 2026

Publicado por primera vez (Actual)

28 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de octubre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

28 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

IPD will not be shared due to participant confidentiality and the potential risk of re-identification in this relatively small, single-institution student sample. Study findings will be reported in aggregate form.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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