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โ† Trials
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Interoceptive Mechanisms of Body Image Disturbance in Anorexia Nervosa

RecruitingNAAges 13 Years - 50 YearsFemaleLaureate Institute for Brain Research, Inc.
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In plain words

What the trial is, and whether it could suit you

The proposed study utilizes a randomized experimental therapeutics design to test a mechanistic framework linking interoceptive processing and disturbed body image, with the purpose of informing the development of future therapies for body image dissatisfaction in anorexia nervosa (AN). A sample of 102 participants will be recruited from the Laureate Eating Disorder Program (LEDP). After being randomized, participants will all receive a one-hour session of acceptance- and mindfulness-based training with a therapist (the introduction session). They will then receive either the interoceptively focused treatment (IFT) or exteroceptively focused treatment (EFT) condition based on randomization. In the IFT condition participants will engage in floatation-REST (Reduced Environmental Stimulation Therapy) while practicing acceptance and mindfulness-based principles. The EFT condition is an exter

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. Primary diagnosis of anorexia nervosa 2. Photographic Figure Rating Scale (PFRS) body dissatisfaction score greater than or equal to 1 3. Eating Disorder Examination Questionnaire (EDE-Q6) Shape Concern Subscale score greater than or equal to 3 4. Weight restored to body mass index (BMI) greater than or equal to 17.5 5. No current evidence of orthostatic hypotension or if there is no evidence of additional fall risk as determined by their provider 6. Clinical status transition from acute to residential status 7. No new psychiatric medications in the week prior to randomization 8. Female sex assigned at birth 9. Ages 13 to 50 years 10. Independently ambulatory 11. Ability to lay flat comfortably 12. English proficiency 13. Willingness and ability to participate in study procedures 14. Provision of informed consent (parent consent and minor assent if less than 18 years of age). Exclusion Criteria: 1. Active suicidal ideation with plan and intent 2. Active cutting or skin lacerating behaviors 3. Pregnancy as defined by urine screening 4. Acute intoxication as indicated by urine drug screen or breathalyzer 5. Orthostatic hypotension as determined by medical provider, evidenced in chart (defined as a drop of โ‰ฅ 20 mmHg in systolic blood pressure (BP) or a drop of โ‰ฅ 10 mm Hg in diastolic blood pressure (BP) when measured shortly after transitioning from lying down to standing). If evidence of orthostasis is present in chart consultation with provider to determine if status creates additional fall risk. If participant is determined to be at increased fall risk (e.g., dizziness upon standing) they will be excluded. 6. Seizure reported within the previous 12 months 7. Co-morbid diagnoses of Diagnostic and Statistical Manual of Mental Disorders, 5th ed. (DSM-5) bipolar disorder, schizophrenia, or other psychosis spectrum disorder 8. Systolic blood pressure \> 160 mmHg 9. Diastolic blood pressure \>100 mmHg 10. Resting heart rate \<50 beats per minute.
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What it tests

  • Floatation-REST
  • IFT
  • EFT
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Where

1 site
Laureate Institute for Brain Research
Tulsa, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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