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Pilot of Reconnecting to Internal Sensations and Experiences in Undergraduates

Not Applicable
Recruiting
Conditions
Suicidal Ideation
Eating Disorder Symptom
Interventions
Behavioral: Healthy Habits
Behavioral: Reconnecting to Internal Sensations and Experiences
Registration Number
NCT05285111
Lead Sponsor
Auburn University
Brief Summary

Project RISE is a randomized control trial. The intervention consists of four modules that focus on multiple aspects of interoception including: body awareness, body sensations/movement, eating, health and self-care, emotional awareness, and understanding the self in relation to others. The comparator condition is called "Health Habits" and is matched for time and attention; participants complete modules related to healthy habits such as financial planning, hygiene, stretching, and healthy eating. Variables of interest include self-report measures of interoception, eating pathology, suicidality, physiological measures of interoception (electrocardiograph; ECG; pain tolerance measured via algometer), and an implicit association test (IAT) with death and life stimuli (meant to measure implicit associations with suicidality). The population will be college students, with current or past suicidality or low interoception.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Low interoceptive awareness
  • History of suicidal ideation or attempt
  • 18 or older
Exclusion Criteria

*Below the age of 18

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Healthy HabitsHealthy HabitsThe comparator condition is called "Health Habits" and is matched for time and attention; participants complete modules related to healthy habits such as financial planning, hygiene, stretching, and healthy eating.
Interoceptive AwarenessReconnecting to Internal Sensations and ExperiencesThe intervention consists of four modules that focus on multiple aspects of interoception including: body awareness, body sensations/movement, eating, health and self-care, emotional awareness, and understanding the self in relation to others.
Primary Outcome Measures
NameTimeMethod
Treatment acceptabilitywithin one week of Post-test

Feasibility and Acceptability questions. Scores range from 4-28. Higher scores indicate a better outcome.

Multidimensional Assessment of Interoceptive Awarenesswithin one week of Post-test

Assessment of Interoceptive Awareness. Total scores range from 0-175. Higher scores indicate a better outcome.

Secondary Outcome Measures
NameTimeMethod
Depression Screening Inventory-Suicidality Subscalewithin one week of Post-test

Measure of suicidal ideation, greater scores indicate more severe ideation. Scores range from 0-12. Higher scores indicate more suicidality, or a worse outcome.

Eating Disorder Examination Questionnairewithin one week of Post-test

Measure of disordered eating. Global score ranges from 0-6; greater scores indicate more severe eating disorder symptoms

Heartbeat perception taskwithin one week of Post-test

Measured via ECG. Perceived versus actual heartbeats are recorded across 3 trials. Scores range from 0-1; higher scores indicate greater cardiac interoceptive accuracy.

Brief Symptom Inventorywithin one week of Post-test

Short measure assessing anxiety and depression symptoms. Scores range from 0-72; greater scores indicate more pathology

Trial Locations

Locations (1)

Auburn University

🇺🇸

Auburn, Alabama, United States

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