Binge Eating DisorderCORNCT07435974
COR Protocol for the Treatment of Binge Eating in Chilean Adults (COR)
A study testing COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food) in people with Binge Eating Disorder and Binge Eating, run by Universidad Catolica de Temuco at 1 site in Chile.
Trial summary
The goal of this clinical study is to learn whether a brief online psychological program called COR can be delivered in a feasible and acceptable way for adults who experience recurrent binge eating. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Binge Eating Disorder, Binge Eating
- What is being tested?
- COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food)
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteChile
- Study dates
- 1 Apr 2026to 30 Jul 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adults aged 18 years or older.
- Overweight or obesity, based on self-report.
- At least three binge-eating episodes in the past 30 days, associated with psychological distress.
- The presence of chronic medical conditions commonly associated with overweight or obesity (e.g., hypothyroidism, hyperthyroidism, dyslipidemia, hypertension, type 2 diabetes mellitus, or polycystic ovary syndrome) is permitted, provided that such conditions are medically stable.
- If present, chronic medical conditions must be medically stable, defined as:
- stable medical treatment for at least 12 weeks,
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- no recent changes in medication,
- no acute clinical decompensation or recent major cardiovascular events,
- at least one related medical follow-up visit in the past 12 months.
- If present, psychopharmacological treatment must be stable, defined as no changes in medication type or dosage during the 12 weeks prior to enrollment.
- Daily access to the internet and to a computer or smartphone that allows participation in online sessions and assessments.
Who cannot join
- Current compensatory behaviors associated with binge eating, such as self-induced vomiting and/or regular use of laxatives, within the past 60 days.
- Pregnancy or breastfeeding at the time of the initial assessment.
- History of bariatric surgery.
- Active suicidal ideation
- Current symptoms consistent with severe mental disorders, such as psychotic disorders, bipolar disorder, complex post-traumatic stress disorder, or severe personality disorders, when associated with marked functional impairment or the need for specialized or higher-intensity clinical care.
- Current substance use pattern that, due to its severity or functional impact, requires specialized clinical treatment.
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- Ongoing psychological and/or nutritional treatment at the time of enrollment, defined as regular sessions or an active treatment plan, regardless of treatment focus or therapeutic approach.
- Presence of active or medically unstable conditions, characterized by clinically significant symptoms, lack of medical follow-up, or recent changes in medication, that could interfere with participation in the intervention or substantially affect eating behavior or mood.
- Significant functional impairment that, in the clinical judgment of the research team, would limit the participant's ability to engage safely and consistently in the intervention.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Chile1 site, 1 recruiting
- Recruiting
Universidad Católica de Temuco
Temuco, La Araucanía, 4780000
Neli Escandon, PhD, 452685078, nescandon@uct.cl
About this study
Official title: A Pilot Study on the Feasibility and Acceptability of the COR (Body Compassion-Emotional Regulation-Conscious Reconnection With Eating) Protocol for Addressing Binge Eating in Chilean Adults
The goal of this clinical study is to learn whether a brief online psychological program called COR can be delivered in a feasible and acceptable way for adults who experience recurrent binge eating.
The main questions this study aims to answer are:
Read more
- Is the COR program acceptable to participants, in terms of satisfaction, adherence, and dropout rates?
- Is the COR program feasible to deliver online, including recruitment, retention, and completion of sessions and questionnaires?
- Do participants show preliminary changes over time in binge eating-related distress and emotional well-being?
Participants in this study are adults who experience recurrent episodes of binge eating. They will take part in an individual online intervention that includes eight weekly sessions, a brief pre-session, and a follow-up session one month after the end of treatment.
During the study, participants will:
- Attend weekly online sessions focused on understanding binge eating, emotions, and the relationship with food and the body
- Practice simple exercises to help manage emotional distress and food-related urges
- Complete short questionnaires before, during, and after the intervention to describe their experiences
The information from this study will help researchers understand whether this type of intervention can be used in future, larger studies and in real-world clinical settings.
Read the detailed description
This study evaluates the COR protocol (Body Compassion-Emotional Regulation-Conscious Reconnection with Food), a brief, manualized psychological intervention designed for adults who experience recurrent binge eating. The study is conducted as a pilot trial to examine implementation-related outcomes and to explore preliminary clinical changes over time.
The COR protocol was developed by integrating evidence-informed components from cognitive-behavioral therapy for eating disorders, dialectical behavior therapy skills, and approaches that promote a more conscious and flexible relationship with eating. The intervention is grounded in a non-weight-centered framework and places emphasis on emotional regulation, experiential work with urges and cravings, and the gradual development of a more compassionate relationship with the body and eating.
The intervention is delivered individually in an online format and consists of eight weekly sessions, preceded by a brief pre-session and followed by a one-month follow-up session. Sessions follow a structured but flexible progression, organized around a defined trajectory of change. Early sessions focus on establishing a therapeutic framework, understanding binge eating as a functional and emotionally driven behavior, and identifying personal vulnerability patterns. Middle sessions emphasize skills for relating differently to urges and emotional distress, including experiential and regulation-based strategies. Later sessions focus on body-related self-criticism, compassion-based practices, consolidation of skills, and planning for continuity of care and relapse prevention.
Each session includes a combination of psychoeducation, guided experiential exercises, reflective discussion, and brief between-session practices. Between-session tasks are designed to support observation and reflection rather than performance or compliance, and difficulties completing tasks are addressed as clinically meaningful information rather than treatment failure.
The protocol is manualized to support consistency across providers while allowing controlled clinical flexibility in pacing, examples, and depth of exploration, according to participant needs. Core components of each session and overarching therapeutic principles are defined as non-modifiable to preserve fidelity to the model.
As part of the study design, the COR protocol is implemented by psychologists with general clinical training who receive structured training in the model prior to implementation, as well as ongoing weekly clinical supervision during the intervention period. Therapist adherence to the protocol is supported through the use of structured adherence checklists, which are intended for monitoring and quality assurance rather than performance evaluation.
This pilot study focuses on outcomes related to feasibility and acceptability of the intervention when delivered online, including aspects of recruitment, retention, adherence, and participant satisfaction. In addition, the study explores preliminary changes over time in binge eating-related symptoms and associated emotional and psychological processes. Data from this pilot will be used to inform refinements to the protocol and the design of future larger-scale studies.
- Conditions
- Binge Eating Disorder, Binge Eating
- Being tested
- COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food)
- Keywords
- Binge eating, Binge Eating Disorder, Body compassion, Emotion regulation, Intuitive eating
- Medical subject headings
- Binge-Eating Disorder, Bulimia, Emotional Regulation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food)Behavioural
The COR protocol (Body Compassion-Emotional Regulation-Conscious Reconnection with Food) is a brief, manualized psychological intervention designed to address recurrent binge eating in adults. The intervention is delivered individually in an online format and consists of eight weekly sessions, preceded by an initial pre-session and followed by a one-month follow-up session.
COR integrates elements from cognitive-behavioral therapy for eating disorders, dialectical behavior therapy skills, and principles of intuitive eating, within a non-weight-centered and compassion-focused framework. The intervention targets key psychological processes involved in binge eating, including emotional regulation, responses to food-related urges and cravings, and the development of a more compassionate relationship with the body and eating.
Sessions include psychoeducation, functional analysis of binge episodes, experiential exercises, brief regulation practices, and reflective between-session activities.
| Study group | Role | What they receive |
|---|---|---|
| COR Protocol | Experimental | Not described Receives: Behavioral: COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of Eligible Participants Who Initiate the COR Intervention
Recruitment rate is defined as the proportion of eligible individuals who begin the COR intervention, calculated as the number of eligible participants who start the intervention divided by the number of eligible individuals who were successfully contacted and formally invited to participate during the recruitment period.
Measured: At enrollment.
Proportion of Participants Who Complete All Eight COR Intervention Sessions
Retention during the intervention is defined as the proportion of participants who complete all eight scheduled COR intervention sessions.
Measured: Up to 8 weeks.
Proportion of Participants Who Attend the 1-Month Follow-Up Session After Completing the COR Intervention
Retention at follow-up is defined as the proportion of participants who completed the eighth COR intervention session and subsequently attended the 1-month follow-up session.
Measured: Up to 12 weeks.
Proportion of Participants Who Discontinue the COR Intervention Before Completing All Eight Sessions
Dropout rate is defined as the proportion of participants who discontinue the COR intervention before completing all eight scheduled sessions. When available, participants' self-reported reasons for discontinuation will be recorded descriptively.
Measured: Up to 8 weeks.
Proportion of Scheduled Assessment Instruments Completed by Participants
Assessment completeness is defined as the proportion of scheduled assessment instruments completed by participants relative to the total number of instruments planned. This includes both formal assessment batteries administered at predefined study time points and weekly monitoring measures collected during the intervention period. This outcome evaluates the feasibility of data collection procedures.
Measured: From baseline through 12 weeks.
Acceptability of the COR Protocol Among Participants and Interventionists
Acceptability of the COR protocol will be assessed using both participant- and interventionist-reported indicators. Participant acceptability will be assessed at post-treatment using the Client Satisfaction Questionnaire (CRES-4), which captures overall satisfaction with the intervention and perceived usefulness. Participant experiences regarding the intervention format, duration, contents, and strategies will be further explored through semi-structured qualitative interviews conducted after completion of the intervention. Interventionist acceptability will be assessed through semi-structured qualitative interviews focused on perceived adequacy, usability, and fit of the COR protocol within the clinical context.
Measured: At completion of the eighth COR intervention session (session 8).
Implementation Fidelity of the COR Protocol
Implementation fidelity of the COR protocol will be assessed by evaluating whether the intervention is delivered as intended. This includes assessment of (a) adherence to the core contents, objectives, and strategies specified for each session, (b) quality of intervention delivery (e.g., structure, clarity, and consistency with the COR model), and (c) participant exposure to the intervention (dose received), operationalized through session attendance, session duration, and completion of between-session tasks. Fidelity indicators will be primarily collected using a therapist-completed adherence checklist administered after each session, complemented by attendance and session-duration records. Descriptive information regarding implementation challenges and adaptations will also be recorded to support monitoring and future refinement of the protocol.
Measured: From the first COR intervention session (session 1) through completion of the eighth COR intervention session (session 8), assessed over 8 weeks.
Secondary outcomes (5)
Change in Binge-Eating Symptoms
Changes in binge-eating symptoms, including the frequency and severity of binge-eating-related behaviors and associated distress, will be assessed using validated self-report measures, including the Eating Disorder-15 (ED-15) and the Binge Eating Disorder Screener-7 (BEDS-7). In addition to the predefined assessment time points, the ED-15 will be administered weekly during the intervention period for monitoring purposes.
Measured: From baseline through 12 weeks.
Change in General Psychological Distress (CORE-OM)
General psychological distress will be assessed using the Clinical Outcomes in Routine Evaluation - Outcome Measure (CORE-OM), a self-report questionnaire that measures overall psychological distress and well-being. This outcome will be used to describe changes in general distress during and after participation in the COR intervention and to support monitoring of participant well-being.
Measured: From baseline through 12 weeks.
Change in Difficulties in Emotion Regulation (DERS)
Difficulties in emotion regulation will be assessed using the Difficulties in Emotion Regulation Scale (DERS), a self-report questionnaire that measures difficulties in understanding, accepting, and managing emotions. This outcome will be used to describe changes in emotion regulation difficulties following participation in the COR intervention.
Measured: From baseline through 12 weeks.
Change in Body Compassion
Changes in body compassion will be assessed using the Body Compassion Scale (BCS), a self-report measure designed to assess compassionate attitudes toward the body.
Measured: From baseline through 12 weeks.
Change in Emotional Eating
Changes in emotional eating will be assessed using the emotional eating subscale of the Dutch Eating Behavior Questionnaire (DEBQ-EE), a self-report measure of eating in response to emotional states.
Measured: From baseline through 12 weeks.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Feb 2026
- Study start1 Apr 2026
- Primary completion30 Jul 2026 (estimated)
- Study completion30 Jul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Binge Eating DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universidad Catolica de Temuco
- Sponsor type
- University, hospital or other
- Collaborators
- Agencia Nacional de Investigación y Desarrollo
- Responsible party
- Principal investigator, Neli Escandón Nagel, Universidad Catolica de Temuco
- Investigators
- Neli Escandon, PhD, Principal investigator, Universidad Catolica de Temuco
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07435974
- Sponsor's protocol ID
- Fondecyt Iniciacion 11230678
- Acronym
- COR
- Status last verified
- Apr 2026
- First submitted
- 12 Feb 2026
- Last updated
- 22 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be shared due to the sensitive nature of the data collected (mental health and eating-related behaviors), the small sample size of this pilot study, and the lack of explicit participant consent for data sharing.
Study at a glance
From the registry record, last updated by the sponsor on 22 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Pilot Study on the Feasibility and Acceptability of the COR (Body Compassion-Emotional Regulation-Conscious Reconnection With Eating) Protocol for Addressing Binge Eating in Chilean Adults
- ClinicalTrials.gov ID
- NCT07435974
- Acronym / sponsor ID
- COR / Fondecyt Iniciacion 11230678
- Conditions
- Binge Eating Disorder, Binge Eating
- Keywords
- Binge eating, Binge Eating Disorder, Body compassion, Emotion regulation, Intuitive eating
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- Universidad Catolica de TemucoUniversity, hospital or other
- Collaborators
- Agencia Nacional de Investigación y Desarrollo
- Study start
- 1 Apr 2026 (actual)
- Primary completion
- 30 Jul 2026 (estimated)
- Study completion
- 30 Jul 2026 (estimated)
- First posted
- 27 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical study is to learn whether a brief online psychological program called COR can be delivered in a feasible and acceptable way for adults who experience recurrent binge eating.
The main questions this study aims to answer are:
- Is the COR program acceptable to participants, in terms of satisfaction, adherence, and dropout rates?
- Is the COR program feasible to deliver online, including recruitment, retention, and completion of sessions and questionnaires?
- Do participants show preliminary changes over time in binge eating-related distress and emotional well-being?
Participants in this study are adults who experience recurrent episodes of binge eating. They will take part in an individual online intervention that includes eight weekly sessions, a brief pre-session, and a follow-up session one month after the end of treatment.
During the study, participants will:
- Attend weekly online sessions focused on understanding binge eating, emotions, and the relationship with food and the body
- Practice simple exercises to help manage emotional distress and food-related urges
- Complete short questionnaires before, during, and after the intervention to describe their experiences
The information from this study will help researchers understand whether this type of intervention can be used in future, larger studies and in real-world clinical settings.
Detailed description
This study evaluates the COR protocol (Body Compassion-Emotional Regulation-Conscious Reconnection with Food), a brief, manualized psychological intervention designed for adults who experience recurrent binge eating. The study is conducted as a pilot trial to examine implementation-related outcomes and to explore preliminary clinical changes over time.
The COR protocol was developed by integrating evidence-informed components from cognitive-behavioral therapy for eating disorders, dialectical behavior therapy skills, and approaches that promote a more conscious and flexible relationship with eating. The intervention is grounded in a non-weight-centered framework and places emphasis on emotional regulation, experiential work with urges and cravings, and the gradual development of a more compassionate relationship with the body and eating.
The intervention is delivered individually in an online format and consists of eight weekly sessions, preceded by a brief pre-session and followed by a one-month follow-up session. Sessions follow a structured but flexible progression, organized around a defined trajectory of change. Early sessions focus on establishing a therapeutic framework, understanding binge eating as a functional and emotionally driven behavior, and identifying personal vulnerability patterns. Middle sessions emphasize skills for relating differently to urges and emotional distress, including experiential and regulation-based strategies. Later sessions focus on body-related self-criticism, compassion-based practices, consolidation of skills, and planning for continuity of care and relapse prevention.
Each session includes a combination of psychoeducation, guided experiential exercises, reflective discussion, and brief between-session practices. Between-session tasks are designed to support observation and reflection rather than performance or compliance, and difficulties completing tasks are addressed as clinically meaningful information rather than treatment failure.
The protocol is manualized to support consistency across providers while allowing controlled clinical flexibility in pacing, examples, and depth of exploration, according to participant needs. Core components of each session and overarching therapeutic principles are defined as non-modifiable to preserve fidelity to the model.
As part of the study design, the COR protocol is implemented by psychologists with general clinical training who receive structured training in the model prior to implementation, as well as ongoing weekly clinical supervision during the intervention period. Therapist adherence to the protocol is supported through the use of structured adherence checklists, which are intended for monitoring and quality assurance rather than performance evaluation.
This pilot study focuses on outcomes related to feasibility and acceptability of the intervention when delivered online, including aspects of recruitment, retention, adherence, and participant satisfaction. In addition, the study explores preliminary changes over time in binge eating-related symptoms and associated emotional and psychological processes. Data from this pilot will be used to inform refinements to the protocol and the design of future larger-scale studies.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| COR Protocol | Experimental | Behavioral: COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (11 listed)
- Adults aged 18 years or older.
- Overweight or obesity, based on self-report.
- At least three binge-eating episodes in the past 30 days, associated with psychological distress.
- The presence of chronic medical conditions commonly associated with overweight or obesity (e.g., hypothyroidism, hyperthyroidism, dyslipidemia, hypertension, type 2 diabetes mellitus, or polycystic ovary syndrome) is permitted, provided that such conditions are medically stable.
- If present, chronic medical conditions must be medically stable, defined as:
Key exclusion criteria (9 listed)
- Current compensatory behaviors associated with binge eating, such as self-induced vomiting and/or regular use of laxatives, within the past 60 days.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food)The COR protocol (Body Compassion-Emotional Regulation-Conscious Reconnection with Food) is a brief, manualized psychological intervention designed to address recurrent binge eating in adults. The intervention is delivered individually in an online format and consists of eight weekly sessions, preceded by an initial pre-session and followed by a one-month follow-up session. COR integrates elements from cognitive-behavioral therapy for eating disorders, dialectical behavior therapy skills, and principles of intuitive eating, within a non-weight-centered and compassion-focused framework. The intervention targets key psychological processes involved in binge eating, including emotional regulation, responses to food-related urges and cravings, and the development of a more compassionate relationship with the body and eating. Sessions include psychoeducation, functional analysis of binge episodes, experiential exercises, brief regulation practices, and reflective between-session activities. | Behavioural | COR Protocol |
Primary outcome
Proportion of Eligible Participants Who Initiate the COR Intervention
Time frame: At enrollment.
Recruitment rate is defined as the proportion of eligible individuals who begin the COR intervention, calculated as the number of eligible participants who start the intervention divided by the number of eligible individuals who were successfully contacted and formally invited to participate during the recruitment period.
Proportion of Participants Who Complete All Eight COR Intervention Sessions
Time frame: Up to 8 weeks.
Retention during the intervention is defined as the proportion of participants who complete all eight scheduled COR intervention sessions.
Proportion of Participants Who Attend the 1-Month Follow-Up Session After Completing the COR Intervention
Time frame: Up to 12 weeks.
Retention at follow-up is defined as the proportion of participants who completed the eighth COR intervention session and subsequently attended the 1-month follow-up session.
Proportion of Participants Who Discontinue the COR Intervention Before Completing All Eight Sessions
Time frame: Up to 8 weeks.
Dropout rate is defined as the proportion of participants who discontinue the COR intervention before completing all eight scheduled sessions. When available, participants' self-reported reasons for discontinuation will be recorded descriptively.
Proportion of Scheduled Assessment Instruments Completed by Participants
Time frame: From baseline through 12 weeks.
Assessment completeness is defined as the proportion of scheduled assessment instruments completed by participants relative to the total number of instruments planned. This includes both formal assessment batteries administered at predefined study time points and weekly monitoring measures collected during the intervention period. This outcome evaluates the feasibility of data collection procedures.
Acceptability of the COR Protocol Among Participants and Interventionists
Time frame: At completion of the eighth COR intervention session (session 8).
Acceptability of the COR protocol will be assessed using both participant- and interventionist-reported indicators. Participant acceptability will be assessed at post-treatment using the Client Satisfaction Questionnaire (CRES-4), which captures overall satisfaction with the intervention and perceived usefulness. Participant experiences regarding the intervention format, duration, contents, and strategies will be further explored through semi-structured qualitative interviews conducted after completion of the intervention. Interventionist acceptability will be assessed through semi-structured qualitative interviews focused on perceived adequacy, usability, and fit of the COR protocol within the clinical context.
Implementation Fidelity of the COR Protocol
Time frame: From the first COR intervention session (session 1) through completion of the eighth COR intervention session (session 8), assessed over 8 weeks.
Implementation fidelity of the COR protocol will be assessed by evaluating whether the intervention is delivered as intended. This includes assessment of (a) adherence to the core contents, objectives, and strategies specified for each session, (b) quality of intervention delivery (e.g., structure, clarity, and consistency with the COR model), and (c) participant exposure to the intervention (dose received), operationalized through session attendance, session duration, and completion of between-session tasks. Fidelity indicators will be primarily collected using a therapist-completed adherence checklist administered after each session, complemented by attendance and session-duration records. Descriptive information regarding implementation challenges and adaptations will also be recorded to support monitoring and future refinement of the protocol.
5 secondary outcomes
Change in Binge-Eating Symptoms
Time frame: From baseline through 12 weeks.
Change in General Psychological Distress (CORE-OM)
Time frame: From baseline through 12 weeks.
Change in Difficulties in Emotion Regulation (DERS)
Time frame: From baseline through 12 weeks.
Change in Body Compassion
Time frame: From baseline through 12 weeks.
Change in Emotional Eating
Time frame: From baseline through 12 weeks.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Apr 2026.
- Individual participant dataSharing planned: No. Individual participant data will not be shared due to the sensitive nature of the data collected (mental health and eating-related behaviors), the small sample size of this pilot study, and the lack of explicit participant consent for data sharing.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Neli Escandon, PhD principal investigator
Universidad Catolica de Temuco
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing COR Protocol (Body Compassion - Emotional Regulation - Conscious Reconnection with Food) in people with Binge Eating Disorder and Binge Eating, run by Universidad Catolica de Temuco at 1 site in Chile.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 11 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 22 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Chile. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Neli Escandon, PhD (+56452685078, nescandon@uct.cl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Proportion of Eligible Participants Who Initiate the COR Intervention (time frame: At enrollment.). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2026.