Heart Rate Sensing and Response in Persons With Anorexia Nervosa



Status:Recruiting
Conditions:Psychiatric, Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 35
Updated:4/21/2016
Start Date:March 2016
End Date:January 2017
Contact:Lucy W Piner, MS
Email:lucy.piner@dm.duke.edu
Phone:919-660-6781

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There are two major goals of this investigation. First, to develop pilot data to justify a
larger randomized clinical trial of an intervention designed to train interoceptive signals
(IS) and interoceptive responsivity (IR) in persons with Anorexia Nervosa (AN). Second, the
investigators will determine whether persons with AN have similar or different IS and IR for
heart rate while exercising as compared to age and gender matched controls.

The purpose of this pilot investigation is to assess AN interoceptive sensitivity and
responsivity as it pertains to heart rate during exercise. Thirty adults, 18 years and older
will be recruited for a cross-sectional comparison of IS and IR in the context of exercise.

Inclusion Criteria: Study participants will include adults with anorexia spectrum
disorders and healthy age and gender matched controls. There will be two control groups,
one that includes regularly exercising age and gender matched persons and one where
controls do not engage in regular exercise.

For those with AN, the following INCLUSION criteria must be met:

- Age 18 to 35 years

- BMI 25 kg/m2 or less

- Diagnosis of anorexia spectrum disorder

- Medications: Stable use of all medications ≥ three months

For age and gender matched controls, the following INCLUSION criteria must be met:

- Age 18 to 35 years

- BMI 25 kg/m2 or less

- No diagnosis of anorexia spectrum disorder

- Medications: Stable use of all medications ≥ three months

- Age (+/- 2 years) and gender matched to study participant

Exclusion Criteria:

- History of diabetes, heart disease or taking medications for those conditions

- History of hypertension (high blood pressure) not controlled with medication

- Orthopedic limitations, musculoskeletal disease and/or injury

- Inability to consent

- Lack of transportation to the Duke Center for Living campus
We found this trial at
1
site
Durham, North Carolina 27705
Principal Investigator: Kim M Huffman, MD
Phone: 919-660-6781
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mi
from
Durham, NC
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