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RECRUITING NA

Optimizing Digital Health Technology Interventions to Increase Skill Acquisition and Utilization

NCT05473013 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to identify the independent and combined effects of two types of self-monitoring and two types of micro-interventions when combined with standard cognitive behavioral treatment for bulimia nervosa (BN) and binge eating disorder (BED). The primary aims of this study are (1) to evaluate the optimal complexity of Self-Monitoring and Micro-Interventions on eating pathology (at post-treatment and at 6 and 12-month follow-ups and (2) to test the hypotheses that the optimal complexity level of each component is moderated by baseline deficits in self-regulation. The secondary aim will be to test target engagement for each level of complexity for each component, i.e., to test whether higher complexity of each technological components is associated with better rates of therapeutic skill use and acquisition and that improvements in skill use and acquisition are associated with improvements in outcomes. A final exploratory aim will be to quantify the component interaction effects, which may be partially additive (because components overlap and/or there is diminishing return), fully additive, or synergistic (in that component complexities may partially depend on each other).

Interventions

  • BEHAVIORAL Behavioral Therapy for Eating Disorders
  • BEHAVIORAL Skills Monitoring On
  • BEHAVIORAL Automated Reminder Messages
  • BEHAVIORAL JITAIs

Study Locations (1)

Pennsylvania

  • Drexel University, Stratton Hall — Philadelphia

Trial Details

FieldValue
Enrollment Target 264 participants
Start Date 2023-01-06
Est. Completion 2026-03
Phase NA

Sponsor

Drexel University

65 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05473013

The ClinicalTrials.gov registry entry for NCT05473013 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 264 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Drexel University, which has 65 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Bulimia Nervosa appearing as the primary indexed condition, and to 4 interventions — of which Behavioral Therapy for Eating Disorders is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05473013 reports 1 study location spanning 1 distinct geographic area — top geographies include Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05473013 about?

NCT05473013 is a clinical study titled "Optimizing Digital Health Technology Interventions to Increase Skill Acquisition and Utilization". The purpose of this study is to identify the independent and combined effects of two types of self-monitoring and two types of micro-interventions when combined with standard cognitive behavioral treatment for bulimia nervosa (BN) and binge eating disorder (BED). The primary aims of this study are (...

What is the current status of trial NCT05473013?

This trial is currently recruiting. It is a NA study. The enrollment target is 264 participants. The study started on 2023-01-06. Estimated completion is 2026-03.

What conditions does trial NCT05473013 study?

This clinical trial studies the following conditions: Bulimia Nervosa, Binge-Eating Disorder, Binge Eating, Bulimia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05473013?

The interventions under investigation include: Behavioral Therapy for Eating Disorders (BEHAVIORAL), Skills Monitoring On (BEHAVIORAL), Automated Reminder Messages (BEHAVIORAL), JITAIs (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05473013?

This trial is sponsored by Drexel University, which has 65 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05473013 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial