Recruiting NA Childhood Obesity

New treatment option for Childhood Obesity

Official title The Dose Trial: Dose Intensity of Behavioral Interventions for Childhood Obesity

ClinicalTrials.gov ID: NCT06654323

What this study is testing

What it's testing
The research team is recruiting 900 children between the ages 5-17 with obesity from Tennessee and Louisiana. The team is assigning children and their caregivers by chance to one of five groups.
  • Time commitment: about 12 months
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 5 to 17

You may be able to join if

  • BMI≥95th percentile for age and sex based on standardized CDC growth curves.
  • parent/caregiver aged ≥ 18 years old
  • are comfortable speaking and reading English or Spanish;
  • are a patient of a participating clinical practice;
  • are able to provide written or verbal consent/assent;

You likely can't join if

  • families for whom the primary care provider (PCP) or site principal investigator (PI) thinks the study and/or intervention is clinically/medically...
  • participant child is taking weight management medications at the time of enrollment;
  • participant child plans to undergo bariatric surgery or another weight loss operation during the 12-month study; or
  • participant caregiver-child dyad has plans to move during the 12-month study and will no longer be a patient of a participating clinic.
See the full eligibility criteria
Who can join
  • BMI≥95th percentile for age and sex based on standardized CDC growth curves.
  • parent/caregiver aged ≥ 18 years old
  • are comfortable speaking and reading English or Spanish;
  • are a patient of a participating clinical practice;
  • are able to provide written or verbal consent/assent;
  • are able to attend scheduled sessions in the 12-month study;
  • are willing to make behavioral and lifestyle changes;
  • are able to access the internet to participate in online intervention components;
  • complete baseline data collection, including child height and weight; and
  • complete at least 90% of baseline survey items no later than 14 days after the baseline visit.
What rules you out
  • families for whom the primary care provider (PCP) or site principal investigator (PI) thinks the study and/or intervention is clinically/medically inappropriate (e.g. developmental delay, disordered eating, mobility...
  • participant child is taking weight management medications at the time of enrollment;
  • participant child plans to undergo bariatric surgery or another weight loss operation during the 12-month study; or
  • participant caregiver-child dyad has plans to move during the 12-month study and will no longer be a patient of a participating clinic.

The study team makes the final eligibility decision.

Where it's taking place

  • Baton Rouge, Louisiana, United States
  • Nashville, Tennessee, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The study runs about 12 months per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.

Who can join this trial?

This study is enrolling all sexes, 5 years to 17 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Baton Rouge, Louisiana, United States; Nashville, Tennessee, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.