Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05655390

iFD-SuRvivE funCtiONal effiCacy and bIologicaL corrElates (RECONCILE Study)

Led by Iria Grande · Updated on 2026-05-12

120

Participants Needed

4

Research Sites

106 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess the effectiveness of an original intervention 'Functional Recovery in Depression and Suicide Risk Prevention Based on Emotion Regulation and Values: A Group Program' (from the original Spanish version: Programa Grupal De Recuperación Funcional En Depresión Y Prevención De Riesgo Suicida Basado En Regulación Emocional Y Valores) in depressed patients who have recently attempted suicide by improving their psychosocial functioning and therefore enhancing their ability to perform activities of daily living. As secondary objectives, the effectiveness of the intervention will be evaluated by determining cognitive performance (particularly decision-making, inhibition, and attention), quality of life, clinical status, and their relationship with neuroimaging correlates. Main target neuroimaging areas include the orbitofrontal cortex and dorsal prefrontal cortex.

CONDITIONS

Official Title

iFD-SuRvivE funCtiONal effiCacy and bIologicaL corrElates (RECONCILE Study)

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years old
  • Having attempted suicide
  • Provide written informed consent
  • No claustrophobia/metallic objects/implants
Not Eligible

You will not qualify if you...

  • Intelligence quotient below 70 and impaired functioning
  • Any medical condition that could affect neuropsychological performance (such as neurological diseases) or a history of head trauma with loss of consciousness
  • Participation in any structured psychological intervention within the past 6 months
  • Patients who received electroconvulsive therapy within the past 6 months
  • Inability to give inform consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Hospital Clínic Barcelona

Barcelona, Barcelona, Spain, 08036

Actively Recruiting

2

Hospital del Mar

Barcelona, Spain

Actively Recruiting

3

Hospital Clínico San Carlos

Madrid, Spain

Actively Recruiting

4

Hospital Gregorio Marañón

Madrid, Spain

Actively Recruiting

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Research Team

I

Iria Grande

CONTACT

N

Natalia Roberto

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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