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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04414553
Other study ID # 20-1337
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 10, 2023
Est. completion date November 3, 2023

Study information

Verified date February 2024
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To address childhood overweight disparities among Latino children in immigrant families a pilot trial of a community-based obesity treatment program, Community Active and Healthy Families (AHF), among 5-12 year old overweight and obese Latino children in immigrant families using pre/post design will be conducted. The hypothesis is that children participating in Community-AHF will demonstrate a reduction in child body mass index as measured by %BMIp95 (primary outcome) and improved diet physical activity behaviors (secondary outcomes) at intervention completion compared with pre-intervention


Description:

To address childhood overweight disparities among Latino children in immigrant families a pilot trial of a community-based obesity treatment program, Community Active and Healthy Families (AHF), among 5-12 year old overweight and obese Latino children in immigrant families using a pre/post design will be conducted. As this is a pilot study, we will not be powered to detect statistically significant differences pre- and post- intervention. We will measure the average change in %BMIp95 between baseline and completion of the Community-AHF active phase. Without a counterfactual (control group) we will not be able assign responsibility to Community-AHF for any observed improvements. Change in %BMIp95 across the study period will provide data to test our hypotheses and will inform statistical power analyses for a subsequent trial. This pre- and post-intervention data is ideal for generating sample size estimates for a larger randomized control trial in the same population. We will conduct within-individual analyses for each outcome of interest. We will only analyze participants who contribute pre and post measures in order to avoid biases that can occur when analyses are conducted with all available data. For each outcome for which a participant contributes pre and post measurements, we will calculate pre and post means, standard deviations, differences in means and the p-value of the difference. We will conduct preliminary analyses of outcomes according to subgroups defined by rate of attendance at intervention sessions. If adequate data are available, we will explore the possibility of a nonresponse analysis.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date November 3, 2023
Est. primary completion date September 23, 2023
Accepts healthy volunteers No
Gender All
Age group 5 Years to 99 Years
Eligibility Inclusion Criteria: - Child age 5-12 years with Parent/Caregiver age of 18 or more years - Child BMI >/= 85th percentile for age - Parent is foreign-born, self identifies as Latino/Hispanic and speaks Spanish - Parental commitment to participate in a 4-month intervention Exclusion Criteria: - Child health condition that prevents diet modification or engaging in physical activity - Child BMI >40kg/m2

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Community Active and Healthy Families
Community-AHF will consist of eight, semimonthly 2-hour group appointments. Community-AHF sessions will target two areas: 1) Practical information regarding importance of healthy behaviors, and 2) Problem-solving skills to overcome barriers to improving diet and increasing physical activity and other related healthy behaviors. Each session covers specific objectives, includes a number of complementary activities and provides participants with take-home materials to facilitate behavior change. Community-AHF will be delivered by a nurse and a Community Health Worker (CHW) trained by a consultant nutritionist and study investigators. The CHW will contact families between group sessions to discuss challenges and successes regarding lifestyle changes.

Locations

Country Name City State
United States University of Colorado Aurora Colorado
United States Johns Hopkins University Baltimore Maryland

Sponsors (2)

Lead Sponsor Collaborator
University of Colorado, Denver Johns Hopkins University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in Total-log activity counts This is an accelerometer-derived measure on a subset of participants that characterizes volume of activity. It is calculated by taking the log of activity counts observed for each minute, adding 1, and then calculating an average value per day. The log transformation of total activity counts results in the improved sensitivity to lower volumes of activity. This measure can be helpful for populations that have low levels of activity and is a continuous measure. Baseline, 4 months,
Other Change in Total Activity Counts This is an accelerometer derived measure that characterizes general volume of physical activity. This is the most commonly used measure to understand accelerometer-derived activity during the day and is a continuous measure. Baseline, 4 months,
Other Change in Active-to-sedentary transition probability This is an accelerometer-derived measure that characterizes fragmentation of physical activity and depends on the frequency of transitioning from active to sedentary state. It is a complementary measure to volume of physical activity. This is a bounded measure between 0-1. Baseline, 4 months,
Primary Change in age- and sex-specific BMI expressed as percent of the 95th percentile (%BMIp95) Child Body Mass Index as calculated from child height and weight measurement to assess change from baseline to 10 month followup Baseline, 4 months
Primary Change in %BMIp95 Trajectory Child %BMIp95 over time as measured at baseline, 4 months Baseline, 4 months
Secondary Change in Child Diet Child diet is measured using the Block Kids Food Screener or selected questions from the School Physical Activity Nutrition Project (only used if Block screener not approved by University Purchasing office as it is licensed). The Block Kids Food Screener is a 41-item food frequency questionnaire developed by NutritionQuest (Berkeley, California, USA). Baseline,4 months
Secondary Change in Child Physical Activity parent-report of the number of days the child is physically active for 60 minutes during a typical week Range 0-7, Higher scores indicate a better outcome (more physical activity) Baseline, 4months
Secondary Change in Parenting Self-Efficacy Change in 4 questions related to self efficacy Range10-60, Higher scores indicate a better outcome (more parenting self efficacy) Baseline, 4 months
Secondary Change in Parent Promotion of Physical Activity/Healthy Eating Questions selected questions from the School Physical Activity and Nutrition Project no established scale but we are planning to create a composite score based on these questions but will need to see the distribution of responses to finalize Baseline, 4 months
Secondary Change in Obesogenic Food Availability in the Home Availability of food in the home that contributes to obesity (high-fat foods, candy, processed meats) determined by home food inventory measure Range: 0-71; lower scores indicate a better outcome (less obesogenic food in the home) Baseline,4 months
Secondary Change in Parent Perceived Stress The 10-item Perceived Stress Score measures global perceived stress experienced across the past 30 days.
Range: 0-40, lower scores indicate a better outcome (less stress)
Baseline, 4 months
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