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NCT05837312 · ClinicalTrials.gov registry record · NA
Testing the Effects of RISE on Eating Pathology
A NA study of Eating Disorder Symptoms, sponsored by Auburn University.
- Active
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT05837312 is a NA study of Eating Disorder Symptoms that is active but no longer recruiting, run by Auburn University. The registered enrollment target is 50 participants. The trial reports 1 study location across 1 state.
The verdict
NCT05837312, a NA study of Eating Disorder Symptoms, is active but no longer recruiting, sponsored by Auburn University.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
Interoception is the process of perceiving one's bodily sensations. Interoception is critical for survival and maintaining homeostasis, as it motivates sensation- and need-specific autonomic reflexes and adaptive behaviors (e.g., eating when hungry, terminating eating upon fullness, drinking when thirsty). Not all individuals have accurate interoceptive abilities. Individuals with eating disorders often have low perception of gastrointestinal, pain, and emotion sensations. Interoceptive dysfunction is believed to influence the development and maintenance of many forms of psychopathology. Identifying effective ways to restore accurate interoceptive processing is an important aim for clinical researchers. The goal of the present study is to continue to test the effectiveness of a training for interoceptive dysfunction that aims to reconnect individuals with eating disorders with their internal sensations, which is called, Reconnecting to Internal Sensations.
Conditions Studied
Interventions
- BEHAVIORAL Reconnecting to Internal Sensations and Experiences
Study Locations (1)
Kentucky
- Louisville Center For Eating Disorders - Louisville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-02-01 |
| Est. Completion | 2027-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05837312
The ClinicalTrials.gov registry entry for NCT05837312 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Auburn University, which has 54 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Eating Disorder Symptoms appearing as the primary indexed condition, and to 1 intervention - of which Reconnecting to Internal Sensations and Experiences is the first listed.
NCT05837312 reports 1 study location spanning 1 distinct geographic area - top geographies include Kentucky.
Frequently Asked Questions
What is clinical trial NCT05837312 about?
NCT05837312 is a clinical study titled "Testing the Effects of RISE on Eating Pathology". Interoception is the process of perceiving one's bodily sensations. Interoception is critical for survival and maintaining homeostasis, as it motivates sensation- and need-specific autonomic reflexes and adaptive behaviors (e.g., eating when hungry, terminating eating upon fullness, drinking when th...
What is the current status of trial NCT05837312?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-02-01. Estimated completion is 2027-12.
What conditions does trial NCT05837312 study?
This clinical trial studies the following conditions: Eating Disorder Symptoms.
What interventions are being tested in trial NCT05837312?
The interventions under investigation include: Reconnecting to Internal Sensations and Experiences (BEHAVIORAL).
Who is sponsoring clinical trial NCT05837312?
This trial is sponsored by Auburn University, which has 54 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05837312 being conducted?
This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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