Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06101810

The Efficacy of Treatments to Improve Self-esteem

Led by GGZ Noord-Holland-Noord · Updated on 2026-01-29

70

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study is to examine the effectivity of two self-esteem interventions (COMET (Korrelboom) and CBT (De Neef)) in a general psychiatric population. The main questions it aims to answer are: * is there a difference between the two interventions in effectiveness on increasing self-esteem? * is there a difference between the two interventions in effect on levels of anxiety, depression and general mental health? * are found effects on levels of anxiety, depression and general mental health associated with changes in self-esteem? * is the ability to use imagination a moderator for outcomes in both conditions? Participants are randomised over both conditions. At baseline (T0), end of treatment (T1) and follow-up at 6 months (T2) several outcome measures are conducted, such as RSES, DASS and MHC-SF.

CONDITIONS

Official Title

The Efficacy of Treatments to Improve Self-esteem

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • A self-perceived low self-esteem established by both patient and caregiver by means of (consent to) referral for self-esteem treatment.
Not Eligible

You will not qualify if you...

  • Severe suicidality requiring hospitalization or other crisis care
  • Acute psychosis
  • Current manic episode
  • Current alcohol or drug abuse
  • Insufficient knowledge of the Dutch language
  • Illiteracy
  • Unable to identify at least one positive aspect of oneself, even if not felt as convincing

AI-Screening

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Trial Site Locations

Total: 1 location

1

Stichting GGZ Noord-Holland-Noord

Heerhugowaard, North Holland, Netherlands, 1703WC

Actively Recruiting

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Research Team

E

Ellen de Jonge, MSc

CONTACT

E

Eva Velthorst, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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