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A Pilot Study of a Remote ADHD Monitoring Program

IDeA States Pediatric Clinical Trials Network · with Medical University of South Carolina, University of Mississippi Medical Center · NCT06743425

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 5–11 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
36
US sites recruiting
2
Study start
February 4, 2025
Record last updated
April 28, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

RAMP is a pilot study examining the use of an Attention-Deficit/Hyperactivity Disorder (ADHD) Monitoring Program during the early stages of treating ADHD in children living in rural settings. This trial will enroll 36 caregiver/infant dyads across 2 sites and will evaluate feasibility endpoints rather than clinical outcomes. Enrolled participants will be randomized 1:1 to the intervention group (RAMP reports) or control group (digital education handouts). The study duration is 10 months, including start-up, enrollment and intervention, and data analysis and manuscript submission.

Being studied: RAMP Reports; Digital Education Handouts

Conditions: Attention-deficit/Hyperactivity Disorder; ADHD

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

The child must

  • be under the care of a participating provider
  • be aged 5-11 at enrollment
  • have a diagnosis of ADHD
  • be initiating stimulant medication for treatment for the first time or have not received stimulant medication for the last 6 months
  • be attending in-person elementary school

The Primary caregiver must

  • be willing and legally able to give consent
  • have access to a smartphone
  • be English-speaking
  • reside with the child at least 3 days per week
  • complete an initial symptom assessment prior to starting stimulant treatment and be willing to provide a copy to the study team

The provider must

  • manage ADHD care in patients age 5-11 years
  • provide informed consent
  • agree to use the RAMP platform if they care for patients randomized to use it
  • agree to provide information to potential participants about the study and contact the research coordinator if interested

Exclusion Criteria

Child

  • has serious mental health comorbidities (Children with depression, anxiety, oppositional defiant disorder will be permitted to participate. Children with schizophrenia, bipolar disorder, conduct disorder and those who have been hospitalized for any mental health condition will be excluded from the study.)
  • has severe neurodevelopment disorders (Children with well-controlled seizure disorders will be permitted to participate.)
  • is currently receiving, or previously received, atypical antipsychotic medication treatment
  • is or becomes pregnant

Recruiting US locations

  • University of Mississippi Medical Center

    Jackson, MS 39216

    Site contact: Hannah Ford, PhD · 601-815-8413 · hford@umc.edu

  • Medical University of South Carolina

    Charleston, SC 29425

    Site contact: Claire MacGeorge, MD · 843-876-8512 · macgeorg@musc.edu

Study contacts (from the official record)

  • Song Ounpraseuth, PhD · 501-686-7233 · STOunpraseuth@uams.edu
  • Kripa Patel, BDS, MPH · (501) 686-5547 · kpatel@uams.edu
All mental health studies in Mississippi →
A Pilot Study of a Remote ADHD Monitoring Program (NCT06743425) | Bored Studies