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ACT-Based Group Therapy and Mobile Application Intervention for Emotional Eating (ACT-EE)

22 aprile 2026 aggiornato da: Merve Sarıtaş Arslan, Saglik Bilimleri Universitesi

The Effect of Acceptance and Commitment Therapy and a Mobile App on Emotional Eating, Emotion Regulation, and Psychological Flexibility in Overweight Individuals

This study aims to evaluate the effects of an Acceptance and Commitment Therapy (ACT)-based group therapy program, combined with an ACT-based mobile app, on emotional eating, emotion regulation, and psychological flexibility in overweight individuals. Emotional eating is a condition in which individuals frequently use eating behavior as a coping mechanism for negative emotions.

Participants will be randomly assigned to intervention groups receiving ACT-based group therapy, ACT-based group therapy combined with an ACT-based mobile app, or a control group. The intervention will last six weeks and will include structured group sessions as well as mobile-based exercises, reminders, and coping strategies.

Outcome measures will include emotional eating, emotion regulation, and psychological flexibility. Assessments will be conducted at baseline, post-intervention, and during the follow-up phase. The findings of this study are expected to contribute to the development of accessible and effective interventions for emotional eating.

Panoramica dello studio

Descrizione dettagliata

Research Objective The aim of this research is to examine the effect of acceptance and commitment therapy and acceptance and commitment therapy-based mobile application use on emotional eating, emotion regulation skills, and psychological resilience levels of overweight individuals. "Research Aim and Type The aim of this research is to examine the effect of acceptance and commitment therapy and acceptance and commitment therapy-based mobile application use on emotional eating, emotion regulation skills, and psychological resilience levels of overweight individuals.

The research was planned as a prospective, parallel, three-group (1:1:1) randomized controlled trial (RCT).

Research Variables Independent variables: Sociodemographic characteristics of the participants Dependent variables: Emotional eating, emotion regulation skills, psychological resilience Research Population and Sample The research population consists of individuals with a BMI of 25 and above living in Zonguldak province, Türkiye. The research sample consists of individuals with a Body Mass Index (BMI) of 25 and above who applied to the Nutrition and Dietetics outpatient clinics of Zonguldak Atatürk State Hospital and Zonguldak Karadeniz Ereğli State Hospital. The sample size of the research was calculated using G*Power 3.1.9.7 software. In the calculation made A three-group research design with an effect size of 0.815, a 5% margin of error, and a 95% power level is expected to reach a sample of 66 individuals. Considering the high power of the test and potential losses, the target sample size is 78 individuals. The sample size for each group is calculated as 26 individuals (KCT: 26, KCT+Mobile Application: 26, Waiting List: 26). Research data will be collected using an Information Form, the Emotional Eating Subscale of the Dutch Eating Behavior Questionnaire, the Difficulties in Emotion Regulation Scale (DERS), and the Acceptance and Action Form-II. The researcher has completed a 40-hour theoretical and practical training in 'Acceptance and Commitment Therapy (ACT)' organized by the Association of Contextual Behavioral Sciences and Psychotherapies and the Association of Cognitive Behavioral Psychotherapies. Additionally, the researcher has received four hours of training in the "Emotion Regulation Training Program" organized by Başkent Psychology Workshop and the Addiction Academy. Ethical committee approval required for the research (Date: (Received on 05.03.2025, Number: 36721). Permission was obtained from the Zonguldak Provincial Health Directorate for institutional permissions. Permission was obtained from the authors for the data collection forms used in the research. Individuals participating in the research will be informed in accordance with the Helsinki Declaration and their written and verbal consent will be obtained.

A group therapy intervention program was developed by the researcher in line with the literature. The program was planned with the aim of helping overweight individuals identify the problems they experience with emotional eating and emotion regulation, to define/understand the emotions that cause emotional eating, and to learn to live with these emotions instead of trying to prevent them. The relevant program was submitted to expert opinion, and after expert opinions, the necessary adjustments were made and the final version was prepared. In user-centered applications, the focus is on understanding and adapting to the users' perspective during the development phase of digital interventions. Including users in the process from the planning stage, conducting qualitative interviews, goes beyond evaluating usability and satisfaction and contributes to the creation of the psychosocial context of the intervention. Accordingly, in the second stage, for the design of the mobile application, data was collected from individuals experiencing emotional eating problems and from those with emotional eating, emotion regulation skills, and Experienced psychiatric nurses, psychiatrists, psychologists, and software developers with expertise in mobile application design were consulted regarding the content and design of the mobile application. In the third stage, storyboards were designed by the researcher based on the literature and the opinions received in the second stage. The mobile application included short psychoeducational content on emotional eating and emotion regulation, acceptance and commitment therapy-based emotion monitoring and awareness exercises that participants can use in their daily lives, data entry areas that allow for daily monitoring, progress charts that will enable them to track themselves with weekly analyses, and motivational messages to support and remind them to use the mobile application. After the completion of the mobile application design, it was presented again to expert opinions and the opinions of individuals experiencing emotional eating problems, and simultaneous adjustments were made in line with the suggestions received. Participants will be able to access the mobile application with their personal email addresses and passwords. The researcher will be able to track user data from their own administrator panel. Informed consent forms will be obtained from participants before the mobile application is launched.

Tipo di studio

Interventistico

Iscrizione (Stimato)

78

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Merkez
      • Zonguldak, Merkez, Turchia (Türkiye), 67000
        • Zonguldak Atatürk State Hospital
        • Contatto:
        • Contatto:
        • Investigatore principale:
          • Merve Sarıtaş Arslan, RN Msc
        • Sub-investigatore:
          • elvan emine ata, phD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Agreeing to participate in the study,
  • Being between 18-65 years of age,
  • Having a body mass index ≤ 25 (BMI ≤ 29.9),
  • Being able to read and write,
  • Having an iOS or Android smartphone,
  • Having internet access,
  • Having a home environment suitable for online sessions (having a computer/smartphone, internet access at home, the patient being able to be alone in the room during the session, etc.),

Exclusion Criteria:

  • Having communication problems that would prevent the interview,
  • Having a diagnosis of a mental disorder, including an eating disorder, that would prevent participation in the study, or having concomitant serious medical conditions that could potentially jeopardize study participation.
  • Having undergone bariatric surgery. • Being on the waiting list for bariatric surgery.
  • Being pregnant, breastfeeding, or planning to become pregnant within the next 6 months.
  • Receiving therapy/counseling for emotional eating and emotion regulation problems,
  • Using a mobile application for emotional eating and emotion regulation problems,

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: ACT Group Therapy
Participants in this group will undergo a six-week structured group therapy program based on Acceptance and Commitment Therapy (ACT).
The Acceptance and Commitment Therapy (ACT)-based group therapy program is structured as one session per week for six weeks. Sessions will last 60-90 minutes. The sessions will focus on the core ACT processes: acceptance, cognitive dissociation, being present, contextual self, value identification, and value-oriented action. Psychoeducation, experiential exercises, mindfulness practices, and group sharing will be used during the sessions. Homework and practice tasks will be assigned between sessions to support participants in applying the skills they learn to their daily lives.
Sperimentale: ACT Group Therapy + Mobile Application
Participants in this group will receive six weeks of Acceptance and Commitment Therapy (ACT)-based group therapy, and will have access to an ACT-based mobile application to support the therapy process.
The Acceptance and Commitment Therapy (ACT)-based group therapy program is structured as one session per week for six weeks. Sessions will last 60-90 minutes. The sessions will focus on the core ACT processes: acceptance, cognitive dissociation, being present, contextual self, value identification, and value-oriented action. Psychoeducation, experiential exercises, mindfulness practices, and group sharing will be used during the sessions. Homework and practice tasks will be assigned between sessions to support participants in applying the skills they learn to their daily lives.
The ACT-based mobile application was developed to support the therapy process. The application offers psychoeducational content, ACT-based exercises, reminders, motivational messages, and tools to support the application of skills in daily life. It also allows users to monitor their mood and eating behaviors.
Altri nomi:
  • ACTivity
Nessun intervento: Waitlist Control Group
Participants in this group will be placed on a waiting list and will not receive any intervention during the study. They will have access to the mobile application after the study is completed.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Emotional Eating Level
Lasso di tempo: Baseline, post-intervention (6 weeks), and 3-month follow-up.
Participants' levels of emotional eating will be assessed using a validated and reliable self-report scale. The DEBQ Emotional Eating subscale will be used in the assessment. The scale measures individuals' eating behaviors in response to emotional states such as stress, sadness, and anxiety. Higher scores indicate higher levels of emotional eating behavior.
Baseline, post-intervention (6 weeks), and 3-month follow-up.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Changes in Emotion Regulation Skills
Lasso di tempo: Baseline, post-intervention (6 weeks), and 3-month follow-up.
431 Participants' emotion regulation skills will be assessed using a validated and reliable self-report scale. The scale measures individuals' ability to be aware of emotions, understand emotions, accept emotions, and manage emotional responses. Higher scores indicate increased difficulty in emotion regulation. Emotion regulation will be assessed using the Difficulty in Emotion Regulation Scale (DERS).
Baseline, post-intervention (6 weeks), and 3-month follow-up.
Changes in Acceptance and Action Form-II (AAP-II) Scores
Lasso di tempo: Baseline, post-intervention (6 weeks), and 3-month follow-up.
Participants' levels of psychological resilience will be assessed using the Acceptance and Action Form-II (AAF-II). AAF-II is a self-report-based scale that measures individuals' avoidance tendencies and levels of psychological rigidity in the face of challenging thoughts and feelings. High scores on the scale indicate low psychological resilience, meaning increased psychological rigidity.
Baseline, post-intervention (6 weeks), and 3-month follow-up.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

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Collegamenti utili

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 giugno 2026

Completamento primario (Stimato)

30 settembre 2026

Completamento dello studio (Stimato)

30 dicembre 2026

Date di iscrizione allo studio

Primo inviato

22 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

22 aprile 2026

Primo Inserito (Effettivo)

30 aprile 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 aprile 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

22 aprile 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano IPD

Individual participant data (IPD) sharing has not been decided at this stage. Due to ethical considerations, including participant confidentiality and informed consent procedures, data sharing plans will be evaluated after study completion. Any potential data sharing will involve de-identified data.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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