Study of Efficacy and Safety of WELT-ED for Eating Disorder (WCTP-ED-B-01)

WELT corp134 enrolled

Overview

The purpose of this clinical trial is to evaluate the safety and efficacy of a digital therapeutic device (WELT-ED) based on Cognitive Behavioral Therapy (CBT) for the treatment of eating disorders. The main questions it aims to answer are: * Is WELT-ED as effective as standard treatment in reducing the symptoms of eating disorders? * Is the WELT-ED safe for use in the target population without causing adverse effects? Participants will: * Undergo assessments to determine their baseline health status and severity of eating disorder symptoms. * Use WELT-ED or receive standard treatment as directed for the duration of the study period (8 weeks). * Participate in assessments to monitor changes in their eating disorder symptoms and any potential side effects.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

134

Conditions

Eating Disorders Binge Eating Binge-Eating Disorder

Interventions

WELT-ED (CBT based DTx)DEVICE

The product delivers Cognitive Behavioral Therapy for Eating Disorders (CBT-ED) through a software interface (iOS and Android), designed to engage patients in a structured and interactive manner. It operates by analyzing patterns in the patient's lifestyle and eating data, identifying problematic behaviors associated with their eating disorder. Based on this analysis, the software sets daily learning objectives aimed at fostering positive cognitive and behavioral habits. By providing tailored guidance and support, the product seeks to assist patients in making sustainable changes, ultimately contributing to the improvement of eating disorder symptoms. This approach combines the principles of CBT-ED with the convenience and accessibility of digital technology, offering a personalized therapeutic experience to support patients in their recovery.

Standard TreatmentBEHAVIORAL

In the control group, from screening/baseline (Visit 1) to 8 weeks (Visit 5), counseling and support therapy will be conducted at all visits. Participants can continue taking SSRI medications and other antipsychotic drugs that they were already taking for the treatment of eating disorders during the trial period. However, the intake of any additional antipsychotic drugs, other than those already being taken (including SSRIs), is prohibited during the trial period.

Eligibility

Sex: ALLMin age: 19 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Adults aged between 19 and 65 years * Diagnosed with an eating disorder according to ICD-10. F50.0 Anorexia nervosa F50.1 Atypical anorexia nervosa F50.2 Bulimia nervosa F50.3 Atypical bulimia nervosa F50.4 Overeating associated with other psychological disturbances F50.5 Vomiting associated with other psychological disturbances F50.8 Other eating disorders F50.9 Eating disorder, unspecified) * Have a binge eating frequency (as per item 14 of the EDE-Q) of 4 or more times over the past 4 weeks (28 days) at the time of screening. * Able to use a mobile application (app) on a smartphone without difficulty. * After receiving and understanding sufficient information about this clinical trial, voluntarily decides to participate and provides written consent. Exclusion Criteria: * Previously received Cognitive Behavioral Therapy for the treatment of an eating disorder. * Have a history of bariatric surgery (e.g., adjustable gastric band, sleeve gastrectomy, biliopancreatic diversion, Roux-en-Y gastric bypass). * Have a BMI less than 17 kg/m\^2 or more than 40 kg/m\^2 at the time of screening. * Diagnosed with a major psychiatric disorder according to the MINI. * Have a past or current diagnosis of schizophrenia or bipolar disorder. * At risk of suicide (C-SSRS score of 4 or higher) or have attempted suicide in the past 2 weeks. * Have active and progressive physical illnesses (e.g., congestive heart failure, chronic obstructive pulmonary disease, acute pain), neurological disorders (e.g., cerebrovascular disease), neurodegenerative diseases (e.g., dementia, multiple sclerosis), unstable medical conditions, or a life expectancy of less than 6 months. * Pregnant or planning to become pregnant during the trial period. * Participated in another clinical trial within 4 weeks prior to screening. * Have a history of alcohol or substance abuse. * Considered by the investigator to be unsuitable for participation in this clinical trial for any other reason.

Outcomes

Primary Outcomes

Binge Eating Frequency

Change of Binge Eating Frequency (item 14 of the Eating Disorder Examination Questionnaire, EDE-Q)

Time frame: from baseline (pre-use) to the 8-week point.

Secondary Outcomes

Eating Disorder Examination Questionnaire (EDE-Q)

28 items divided into four subscales: dietary restraint, concern with eating, concern with body shape, and concern with weight. Excluding frequency questions, it assesses symptoms over the past 4 weeks on a 7-point scale from 0 to 6, where higher scores indicate more problematic eating behaviors and attitudes.

Time frame: 8 weeks

Clinical Impairment Assessment (CIA)

Purpose: Evaluates the secondary impairment in three main areas (personal, social, and cognitive) related to eating disorders. Format: A brief self-report tool consisting of 16 items, scored on a 4-point scale from 0 (no impairment) to 3 (high impairment). Interpretation: Total score ranges from 0 to 48, higher scores indicate greater personal, social, and cognitive impairment due to eating disorders.

Time frame: 8 weeks

Patient health questionnaire-9 (PHQ-9)

Purpose: Assesses symptoms of depression based on the diagnostic criteria for major depressive disorder in DSM-IV, focusing on the past two weeks. Format: Comprises 9 questions related to mood, sleep changes, fatigue, appetite change, guilt, worthlessness, concentration difficulty, restlessness, and suicidal thoughts, scored from 0 (not at all) to 3 (nearly every day). Interpretation: Higher scores indicate more severe symptoms of depression.

Time frame: 8 weeks

Generalized anxiety disorder 7-item scale (GAD-7)

Purpose: A screening tool developed to identify symptoms of generalized anxiety disorder, evaluating the severity of related anxiety or worry. Format: Contains 7 items, with responses ranging from 0 (not at all) to 3 (nearly every day). Interpretation: Total scores range from 0 to 21, with higher scores indicating more severe anxiety symptoms and greater functional impairment.

Time frame: 8 weeks

The EuroQol Visual Analogue Scale (EQ-VAS)

Purpose: Measures the participant's overall health status as part of a quality of life questionnaire. Format: A visual analogue scale from 0 to 100. Interpretation: Higher scores represent better overall health status.

Time frame: 8 weeks

Clinical Global Impression of Improvement (CGI-I)

Purpose: Assesses the degree of improvement or worsening in a participant's overall health status at 4 weeks (Visit 3) and 8 weeks (Visit 5). Format: Rated on a 7-point scale, with lower scores indicating greater improvement. Interpretation: Designed to provide a description of change over time, emphasizing the clinician's perspective on patient progress.

Time frame: 8 weeks

Clinical Global Impression of Severity (CGI-S)

Purpose: Evaluates the overall severity of the participant's condition at baseline, 4 weeks (Visit 3), and 8 weeks (Visit 5). Format: A 7-point scale is used, with higher scores indicating greater disease severity. Interpretation: Aims to quantify the severity of the condition from a clinical standpoint, offering insight into the disorder's impact on the patient's life.

Time frame: 8 weeks

Study of Efficacy and Safety of WELT-ED for Eating Disorder (WCTP-ED-B-01)

Overview

Conditions

Interventions

Eligibility

Locations (2)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts