Cognitive Behavioural and Metacognitive Therapy for Low Self-Esteem
Cognitive behavioral therapy
+ Metacognitive therapy
Anxiety Disorders+2
+ Behavior
+ Mental Disorders
Treatment Study
Summary
Study start date: March 1, 2025
Actual date on which the first participant was enrolled.This clinical trial focuses on comparing two types of therapy, Cognitive Behavioural Therapy (CBT) and Meta Cognitive Therapy (MCT), to help people with low self-esteem. Low self-esteem is linked to various mental health issues and can significantly affect one's quality of life. This study is important because it aims to find out which therapy might be more effective in improving self-esteem and mental health outcomes. While CBT has been studied before, MCT is a newer approach that shows promise in treating other disorders, and its effectiveness for low self-esteem has not been thoroughly tested yet. In the study, 20 participants with low self-esteem will be divided into two groups. One group will receive MCT, and the other will undergo CBT. During the study, participants will be evaluated at the start, at the end of the treatment, and six months afterwards to assess changes in their self-esteem and mental health. They will also have weekly assessments to monitor progress. The trial will help determine the accessibility and effectiveness of these therapies and study how the treatments work, aiming to prevent self-esteem issues from returning. There are no specific risks mentioned, but the benefits could lead to better mental health and improved life quality for those with low self-esteem.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Department of Psychology, University of Oslo
Oslo, NorwayOpen Department of Psychology, University of Oslo in Google Maps