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NCT Number: NCT06520657

Addressing Social Determinants of Health in Child Obesity Treatment Using Community Health Workers

The goal of this small pilot study is to test the feasibility of combining a three-month intervention of working with a community health worker (CHW) to address social risk factors for patients prior to beginning a group weight management program for childhood obesity -- Promoting Health in Teens and Kids (PHIT Kids)

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

8 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's Mercy Kansas City

Kansas City, Missouri, 64108, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Family must have one major social risk factor on the Protocol for Responding to & Assessing Patients' Assets, Risks & Experiences (PRAPARE) of the 14 modifiable risk factors
  • Child aged 8 through 12 years of age
  • Child with BMI% at 85th percentile or higher and less than the 120% of the 95th percentile (overweight or class 1 obesity)
  • Child must live with parent/guardian at least 5 out of the 7 days on average (70% of the time)
  • Child and parent able to speak English

Exclusion criteria

  • Child on medications known to cause ongoing weight gain (e.g., atypical anti-psychotics, chronic prednisone, insulin)
  • Child on other medications know to affect weight if dose and BMI z-score has not been stable for 3 months.
  • Diabetes or other disease that has a significant effect on diet, physical activity, or ability to take part in trial activities besides obesity (does not included treated or mild depression or anxiety, limited food allergies or mild physical activity limitations)
  • For parents: new MI, stroke or cancer diagnosis (excluding localized skin cancers) in past 6 months, history of bariatric surgery within the past 3 years, pregnancy in last 6 months or planned within 1 year
  • Child or parent has significant developmental or cognitive impairments or other significant medical issue that would interfere with ability to participate or complete assessment
  • Parent or child has significant physical limitation
  • Parent/child planning to move to from Children's Mercy Kansas City (CMKC) service area

Treatment and study plan

Community Health Worker

Other

Participants are screened for social determinants of health and work with a community health worker for three months to connect them with community and government services to address their family's needs.

Child weight management intervention

Behavioral

This is a 12-week family-based behavioral group intervention to address childhood overweight and obesity.

Standard of Care referral to resources

Other

One-time referral to resources based on need that families can access independently either by providing electronic referral to or providing written contact information for a community resource.

Primary outcomes

  1. Enrollment Rate

    Time frame: 1 year

    Number of participants enrolled (consented) per month

  2. Retention

    Time frame: 6 months

    Attendance at 6 month data assessment

  3. Satisfaction with Community Health Worker (CHW)

    Time frame: 3 months

    A 15-item scale asks about quality of interactions and satisfaction with their CHW. Scores range from 15 to 60, with higher scores indicating increased satisfaction.

  4. Satisfaction with PHIT Kids - Parent

    Time frame: 6 months

    A single 10-point Likert scale satisfaction rating about the group weight management intervention. Scores range from 1-10 with higher scores indicating increased satisfaction.

  5. Child Body Mass Index (BMI) Z-Score

    Time frame: Change in BMI Z-score over a 6 month time period in the child with obesity or overweight

    6 months

  6. Inhibitory Control and Attention

    Time frame: 3 months

    The Flanker Inhibitory and Control Attention Test (Flanker) measures accuracy and reaction time to produce a combined score ranging from 0-10 with higher scores indicating better inhibitory control and attention.

  7. Working Memory

    Time frame: 3 months

    The List Sorting Working Memory Test asks participants to recall a list of foods and animals in order from smallest to largest. Correct responses range from 0-26, and are then converted to nationally normed standard scores ranging from 59-140, with higher scores indicating better working memory.

  8. Cognitive Flexibility

    Time frame: 3 months

    The Dimensional Change Card Sort Test (DCCS) measures accuracy and reaction time to produce a combined score ranging from 0-10 with higher scores indicating better cognitive flexibility.

  9. Parent Cognitive Capacity

    Time frame: 3 months

    The Raven's 2 Progressive Matrices- Digital Short Form (Raven's 2) tests fluid intelligence by asking participants to identify missing pieces in visual geometric patterns of up to 24 progressively more difficult trials. The total number correct is converted into Standard Scores, which will be compared to a participant's other scores over the course of the study. Standard scores range from 59-140 with higher scores indicating increased cognitive capacity.

Secondary outcomes

  1. PHIT Kids attendance

    Time frame: 6 months

    percent of PHIT Kids sessions attended

  2. Percentage of needs met or partially met

    Time frame: 3 months

    At 3 months, participants will review each need identified at baseline and report if they received "All the help I needed," "Most of the help I needed," "A little of the help I needed," or "None of the help I needed." The total number of needs that were at least partially met ("a little", "most" or "all") or that were fully met ("all") will be divided by the total number of needs at baseline

  3. Enrollment in at least one new resource

    Time frame: 3 months

    Yes/No. Family has accessed at 3 months at least one new community or government resource since baseline. Participants will review a list of resources potentially offered to CHW clients and respond whether they currently receive this resource at baseline and 3 months

  4. Number of key measures completed

    Time frame: 6 months

    Number of the following measures completed - outcome measures (child BMI-z, parent weight, MVPA (actigraph; at least 4 days), dietary measures (3 recalls)), bandwidth measures (executive functions measures and Raven matrices) and self-efficacy.

  5. Parent Weight

    Time frame: 6 months and 12 months

    Change in parent weight at 6 month and 12 months

  6. Child Moderate to Vigorous Physical Activity (MVPA)

    Time frame: 6 months and 12 months

    Minutes per week in moderate to vigourous physical activity as measure by an Actigraph waist accelerometer worn by the child. Also percent of time in MVPA

  7. Child Dietary Intake

    Time frame: 6 months and 12 months

    Three 24 hour recalls completed by parent using the he Automated Self-Administered 24-hour Dietary Assessment Tool (ASA 24) computer program - used to calculate fruit and vegetable (FV) servings, sugar sweetened beverages, and number of high fat/high sugar foods (foods with >7g of fat and/or 12g of sugar)

  8. Self-Efficacy

    Time frame: 6 months

    10-item, 5-point Likert scale. Measured by the General Self-Efficacy Scale in the NIH Toolbox. This scale assesses an individual's perceived ability to cope with stressful situations. Scores range from 10 to 50 with higher scores indicating higher self-efficacy.

Sponsors and collaborators

Lead sponsor

Children's Mercy Hospital Kansas City

Other

Collaborators

  • Community Health Council of Wyandotte County
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • University of Kansas Medical Center

Registry information

Official study title

Addressing Social Determinants of Health in Child Obesity Treatment Using Community Health Workers: the Role of Parental Bandwidth in Treatment Effectiveness

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jul 25, 2024
Registry last updated
Jul 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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