Mobile Regulation of Craving Training (mROC-T) to Improve Dietary Intake in Rural Adolescent Girls (NCT06723028) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Mobile Regulation of Craving Training (mROC-T) to Improve Dietary Intake in Rural Adolescent Girls
United States150 participantsStarted 2025-02-01
Plain-language summary
The goal of this clinical trial is to test if a regulation of craving training intervention in the form of a mobile phone app can increase fruit and vegetable intake in adolescent girls ages 14-18 years of age. The main questions it aims to answer are:
1. What is the effect of a mobile app version of the regulation of craving training intervention on healthy eating index scores over one year?
2. What is the effect of a mobile app version of the regulation of craving training intervention on body mass index, waist circumference, and blood glucose over one year? Researchers will compare the active regulation of craving training arm to a control fun food fact arm to see if the regulation of craving training improves HEI scores, BMI, and blood glucose over a year. Participants will be asked to play the regulation of craving training mobile app twice a week for a year.
Who can participate
Age range
15 Years – 18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Biologically female
* Female gender
* Between the ages of 15y and 18y
Exclusion Criteria:
* Biologically male
* Self-identify as male
* BMI percentile (for age and sex) \< 5th%
* Diagnosis from a medical profession of any of the following conditions, syndromes, diseases that may affect growth, glucose metabolism, blood clotting, cognitive development\*:
* Any form of or history of cancer
* Any form of diabetes (type I, II, insipidus)
* Precocious puberty
* Crohn's disease
* Congenital heart defect
* Cystic fibrosis
* Cerebral palsy
* Anorexia nervosa
* Bulimia nervosa
* Active infection
* Fever
* Hemophilia
* Hydrocephalus
* intestinal atresia
* Jeune syndrome
* Klippel-Trénaunay syndrome
* Legg-Calvé-Perthes
* Long QT syndrome
* Muenke syndrome
* Myelomeningocele
* Necrotizing Enterocolitis
* Neutropenia
* Non-alcholoic fatty liver diease
* Pfeiffer Syndrome
* Saethre-Chotzen syndrome
* Shwachman-Diamond syndrome
* Spinal muscular atrophy
* Sturge-Weber syndrome
* Ulcerative Colitis
* von Willebrand disease
* Pancreatitis
* Hurler syndrome
* Niemann-Pick disease
* Tay-Sachs disease
* Gaucher disease
* Krabbe disease
* Zellweger syndrome
* Wilson disease
* Brachial Plexus Palsy
* Brain Abscess or Spinal Abscess
* Coarctation of the Aorta
* Aortic stenosis
* Ventricular septal defect
* Patent ductus arteriosus or mitral valve abnormalities
* Congenital Adrenal Hy…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.