Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06932120

Technology-supported Interventions for Prolonged Grief Disorder (PGD)

Led by Universitat Jaume I · Updated on 2026-01-21

141

Participants Needed

2

Research Sites

98 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main aim of this project is to test the efficacy of two formats of delivering an internet- based treatment(GROw) for Prolonged Grief Disorder (PGD) in order to enhance treatment adherence: in a blended format (that combines self-applied treatment online with face-to face sessions with a therapist by videoconference: BF-GROw) and self-applied online format supported by Ecological Momentary Assessment (EMAs) and Ecological Momentary Interventions (EMIs) (iGROw), compared with a waiting list (WL) control group in a community sample of patients with the diagnosis of PGD. The general initial hypothesis is that both treatment conditions (blended format and self-applied format supported by EMAs and EMIs) will significantly produce an improvement in grief symptoms, compared to the WL control group.

CONDITIONS

Official Title

Technology-supported Interventions for Prolonged Grief Disorder (PGD)

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Being at least 18 years old.
  • Meeting diagnostic criteria for Prolonged Grief Disorder based on the International Classification of Diseases 11 edition (ICD-11).
  • Signing an informed consent.
  • Ability to understand and read Spanish.
  • Ability to use a computer.
  • Having an e-mail address.
  • Having an internet connection and access to a smartphone.
Not Eligible

You will not qualify if you...

  • Presence of high risk of suicide.
  • Presence of severe Axis I mental disorders including substance abuse or dependence, psychotic disorder, dementia, bipolar disorder.
  • Presence of severe personality disorder or medical illness preventing treatment.
  • Receiving other psychological treatment during the study.
  • Increase or change in medication during the study period if receiving pharmacological treatment.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Universitat Jaume I

Castellon, Castellón de La Plana, Spain, 12071

Actively Recruiting

2

Universitat Jaume I

Castellon, Castellón, Spain, 12071

Not Yet Recruiting

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Research Team

S

Soledad Quero, Ph.D and psychology

CONTACT

L

Laura De la Coba Cañizares, Psychology

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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