Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Effects of the Integrated Grief Therapy on Psychological Resilience, Post-Traumatic Growth, Traumatic Stress, and Grief Processes in Earthquake Survivors

8 juni 2026 bijgewerkt door: Burçin Çakır, Sakarya University

Effects of the Integrated Grief Therapy on Earthquake Survivors

This study evaluates the effectiveness of an Integrated Grief Therapy (IGT) group program for adults affected by the February 6, 2023 earthquake in Türkiye. Many earthquake survivors experience psychological difficulties such as traumatic stress, grief, and reduced resilience after losing loved ones, homes, and a sense of safety. This study aims to determine whether a structured group-based therapy program can help improve psychological well-being and reduce distress.

A total of 190 adult participants who experienced the earthquake were included in the study. Participants were randomly assigned to either an experimental group or a waitlist control group. The experimental group participated in an 8-session Integrated Grief Therapy program delivered face-to-face by trained mental health professionals. The program included psychoeducation about grief, emotional expression, cognitive and behavioral coping strategies, and activities designed to support meaning-making and adaptation after loss. The control group continued to receive routine psychosocial support services available in the community but did not participate in the structured therapy during the study period.

All participants completed standardized psychological assessments before and after the intervention. These assessments measured psychological resilience, post-traumatic growth, grief-related difficulties, and traumatic stress symptoms.

The study aims to determine whether participants who receive the Integrated Grief Therapy program show greater improvements in resilience and post-traumatic growth, and greater reductions in traumatic stress and grief symptoms, compared to those who do not receive the intervention during the same period.

The findings from this study may help inform the development of effective, scalable mental health interventions for individuals affected by large-scale disasters.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

190

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Mersin, Turkije (Türkiye)
        • Psychosocial Support and Grief Therapy Center

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Adults aged 18 to 45 years
  • Individuals who were present in Hatay, Türkiye during the 2023 Türkiye-Syria earthquakes
  • Individuals directly affected by the earthquake
  • Ability to provide informed consent
  • Willingness to participate in group-based psychological intervention sessions

Exclusion Criteria:

  • Current diagnosis of a psychotic disorder or severe mental disorder
  • Severe cognitive impairment or neurological condition
  • Acute suicidal risk requiring immediate intervention or hospitalization
  • Currently receiving intensive psychiatric or psychological treatment
  • Substance use disorder in an acute or severe phase
  • Inability to commit to attending the full intervention program
  • Declined or withdrew informed consent

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Integrated Grief Therapy (IGT)
Participants receiving 8-session group-based Integrated Grief Therapy program
Integrated Grief Therapy (IGT) is a structured, 8-session group intervention developed to support individuals coping with loss after a disaster. The program integrates elements of cognitive-behavioral therapy, humanistic approaches, and grief-focused techniques. It includes psychoeducation about grief, identification and restructuring of maladaptive thoughts, emotional expression, interpersonal sharing, and meaning-making activities such as memory exercises and completion letters. The intervention aims to enhance psychological resilience, promote post-traumatic growth, and reduce traumatic stress and grief symptoms.
Geen tussenkomst: Waitlist Control / Treatment as Usual
Participants receiving routine psychosocial support only

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Psychological Resilience Score
Tijdsspanne: 8 week
Psychological resilience will be assessed using the Psychological Resilience Scale for Adults. Total scores range from 33 to 165, with higher scores indicating greater psychological resilience.
8 week

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Depression Score
Tijdsspanne: 8 week
Depression symptoms will be assessed using the Depression subscale of the Depression Anxiety Stress Scales, a self-report instrument. The subscale consists of 7 items with total scores ranging from 0 to 42. Higher scores indicate greater depression severity.
8 week

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

12 april 2024

Primaire voltooiing (Geschat)

1 augustus 2026

Studie voltooiing (Geschat)

30 september 2026

Studieregistratiedata

Eerst ingediend

11 april 2026

Eerst ingediend dat voldeed aan de QC-criteria

8 juni 2026

Eerst geplaatst (Werkelijk)

11 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

11 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

8 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

Group Therapy Intervention Plan

Title of the intervention:

Structured Group Therapy Program for Individuals Exposed to Trauma and Loss

Purpose of the intervention:

The purpose of this group therapy program is to reduce psychological distress among individuals who have experienced traumatic events and loss, provide a safe environment for emotional sharing, strengthen coping skills, enhance perceived social support, and improve overall psychosocial functioning.

Target group:

Adults experiencing psychological distress following earthquake exposure, displacement, bereavement, uncertainty, grief, and trauma-related experiences.

A separate protocol may be developed for adolescents if needed.

Mode of delivery:

Face-to-face, closed-group format

Group structure:

Each group will consist of 8-12 participants. Each group will be facilitated by one group therapist and one co-facilitator/observer.

Facilitators:

Psychologists or mental health professionals trained in trauma, grief, crisis inter

IPD-tijdsbestek voor delen

Understanding trauma and grief reactions

Objective:

To normalize participants' reactions and provide psychoeducation regarding trauma and grief.

Content:

Common emotional, cognitive, and physical reactions after trauma The individual and variable nature of grief Addressing the question: "Are my reactions normal?" Increasing awareness of symptoms and stress responses

Techniques:

Psychoeducation, group sharing, emotion-awareness exercises

IPD-toegangscriteria voor delen

Inclusion Criteria Age 18 years or older Exposure to trauma, loss, displacement, or related distressing experiences Self-reported psychological distress related to these experiences Willingness to participate in group sessions Ability to attend sessions regularly Provision of informed consent Exclusion Criteria Active psychotic symptoms Severe cognitive impairment Acute suicide risk Severe substance intoxication during participation Clinical instability that would significantly impair participation in a group setting

Participants meeting exclusion criteria will be referred to appropriate mental health services when necessary.

Safety and Ethical Considerations Written or verbal informed consent will be obtained from all participants. Confidentiality will be emphasized at the beginning of the group process. Participants may withdraw from the study/intervention at any time without penalty.

Individuals who experience significant emotional distress during sessions will be assessed individ

IPD delen Ondersteunend informatietype

  • MVO

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren