ClinicalTrials.gg
RecruitingNCT06961591CHEF-IDUpdated Aug 11, 2026

Cooking Skills to Improve Long-Term Weight Loss in Young Adults With Intellectual Disabilities

An interventional study of Weight Loss Plus Cooking and Traditional Weight Loss in Intellectual Disability and Overweight and Obesity, sponsored by University of Kansas Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-08-11.

Sponsored by University of Kansas Medical Center · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started May 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
114
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

The goal of this study is to see if adding hands-on cooking classes to a weight management program (called Chef-ID) helps young adults with intellectual disabilities lose more weight and keep it off compared to a standard weight loss program. The study will last 24 months and include three phases: 6 months of active support, 12 months of maintenance, and 6 months with no contact.

The investigators will look at how much weight participants lose over the first 18 months. Changes in cooking skills, body fat, health markers (like blood pressure and cholesterol), daily living skills, and caregiver stress will be tracked. Finally, factors that might help or prevent weight loss, and how changes in weight and body fat are linked to overall health will be explored.

This research will help inform on how to better support healthy lifestyles for people with intellectual disabilities.

Read the detailed description

This study will compare two different approaches to long-term weight loss in young adults (ages 18-30) with mild-to-moderate intellectual disabilities. One group will follow a traditional weight loss program (called eSLD), while the other will follow the same program plus take part in in-person cooking classes (called eSLD+Chef-ID). A total of 114 participants will be randomly assigned by computer to one of the two groups for a 24-month study, which includes 6 months of active support, 12 months of follow-up, and 6 months with no contact.

All participants will follow a simple diet called the "enhanced stoplight diet" and try to get at least 120 minutes of aerobic exercise and 30 minutes of strength training each week. Participants be given an iPad® with pre-recorded exercise videos, a wearable fitness tracker, and will have monthly Zoom check-ins with a health coach for 18 months.

Those in the eSLD+Chef-ID group will also attend fun, hands-on cooking classes twice a month during the first 6 months and once a month from months 7-18. Participants in the traditional eSLD group will receive short motivational video messages from their coach instead of cooking classes.

Weight will be measured at the beginning, 6, 12, 18, and 24 months. Other health measures like cooking skills, body fat, blood pressure, and caregiver stress will also be collected during lab and home visits. The goal is to find out whether learning to cook helps improve long-term weight loss and overall health in this community.

02

Conditions studied

  • Intellectual Disability
  • Overweight and Obesity

Keywords

  • Weight Loss Maintenance
  • Cooking Skills
  • Weight loss
  • Down syndrome
03

In context

Intellectual Disability

387 studies on the registry are indexed under Intellectual Disability; 105 are open to participants now.

This study's planned enrollment of 114 is above the median of 58 across 248 interventional studies indexed under Intellectual Disability.

Browse Intellectual Disability studies →

Lead sponsor

University of Kansas Medical Center is the lead sponsor of 492 studies on the registry; 110 are open to participants now.

Of its 38 completed or terminated interventional studies of FDA-regulated products, 24 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Diagnosis of mild-to-moderate intellectual disability (ID).
  2. 18-35 years of age.
  3. >24.9, Body weight \<350lbs.
  4. Sufficient functional ability to understand directions, communicate preferences, e.g., foods, wants, and can communicate through spoken language e.g., request more to eat/drink, asks for assistance with food preparation.
  5. Living at home with a parent/guardian, or in a supported living environment with a caregiver who assists with food shopping, meal planning, and meal preparation and agrees to serve as a study partner.
  6. Plan to attend all study required visits over the next 24 mos.

Exclusion criteria

Exclusion Criteria:

  1. Unable to participate in PA.
  2. Insulin dependent diabetes as this condition requires medical monitoring beyond the scope of this study.
  3. Participation in a weight management program involving diet, PA, or pharmacotherapy in the past 6 mos.
  4. Diagnosis of Prader-Willi Syndrome.
  5. Pregnancy during the previous 6 mos., currently lactating or planned pregnancy in the following 24 mos. Participants who become pregnant will be removed from the study and referred to appropriate agencies for consultation.
  6. Serious medical risk, e.g., cancer, recent heart attack, stroke, angioplasty as determined by the PCP.
  7. Unwilling to be randomized.
  8. Unable to participate in small group, in-person instruction.
  9. Use of wheelchair or power chair as primary locomotion.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
114 participants (estimated)

Study arms

  • Experimental
    Weight Loss Plus Cooking

    Behavioral: Weight Loss Plus Cooking

  • Active comparator
    Traditional Weight Loss

    Behavioral: Traditional Weight Loss

Interventions

  • BehavioralWeight Loss Plus Cooking

    Participants in the eSLD+Chef-ID group will follow a healthy eating plan using the enhanced stoplight diet, meet with a health coach once a month on Zoom® using an iPad®, and aim to get 120 minutes of aerobic activity and 30 minutes of strength exercises each week. In addition, they will attend in-person cooking classes-twice a month during the first 6 months and once a month for the next 12 months. In these 60-minute classes, instructors will teach cooking skills, and participants will practice on their own or with a partner, depending on their comfort level. They will learn how to safely use kitchen tools and appliances (like ovens, blenders, knives, and measuring cups) and prepare simple meals or snacks.

    Also known as: eSLD+Chef-ID

  • BehavioralTraditional Weight Loss

    Participants in the eSLD group will follow a healthy eating plan using the enhanced stoplight diet, meet once a month with a health coach on Zoom® using an iPad®, and aim to get 120 minutes of aerobic activity and 30 minutes of strength exercises each week. They will also receive short (2-minute) video messages from their coach-twice a month during the first 6 months and once a month after that. These videos will include feedback on their progress, reminders about their goals, and tips to help them stay on track with healthy eating and exercise.

    Also known as: eSLD

06

What researchers measure

Primary outcomes

  1. Weight Loss Between Arms

    Weight will be measured in duplicate on a calibrated scale after an overnight fast during a laboratory visit at baseline, 6, 12, and 18 mos.

    Time frame: Baseline to 18 months

Secondary outcomes

  1. Changes in Weight

    Weight will be measured in duplicate on a calibrated scale during a laboratory visit after an overnight fast at baseline, 6, 12, and 18 mos and during a home visit at 24 mos.

    Time frame: Baseline to 24 months

  2. Activities of Daily Living

    Activities of Daily Living will be assessed using the 17-item Waisman Activities of Daily Living survey, which was specifically developed for and validated in adolescents and adults with intellectual disabilities. Scores range from 0 to 34, with a higher score indicating increased independence.

    Time frame: Baseline to 24 months

  3. Caregiver Strain

    Caregiver strain will be assessed using the Modified Caregiver Strain Index which measures caregivers' levels of strain, a combination of stress and burden. The index assesses 13 aspects of physical health, family finances, social interactions, time demands, and employment. Scores range from 0 to 26, with a higher score indicating increased caregiver strain.

    Time frame: Baseline to 24 months

  4. Fat Mass

    Body composition will be assessed using dual energy x-ray absorptiometry (DXA -Prodigy Advance Plus, GE, Madison WI). Pregnancy testing will be completed by all females prior to each DXA test. All participants will wear a hospital gown during DXA scans to standardize clothing.

    Time frame: Baseline to 18 months

  5. Fat-free Mass

    Body composition will be assessed using dual energy x-ray absorptiometry (DXA -Prodigy Advance Plus, GE, Madison WI). Pregnancy testing will be completed by all females prior to each DXA test. All participants will wear a hospital gown during DXA scans to standardize clothing.

    Time frame: Baseline to 18 months

  6. Percent Body Fat

    Body composition will be assessed using dual energy x-ray absorptiometry (DXA -Prodigy Advance Plus, GE, Madison WI). Pregnancy testing will be completed by all females prior to each DXA test. All participants will wear a hospital gown during DXA scans to standardize clothing.

    Time frame: Baseline to 18 months

  7. High-density Lipoprotein (HDL)

    Whole blood will be drawn by a trained phlebotomist following a minimum 12-hr. fast and sent to The University of Kansas Health Systems for analysis.

    Time frame: Baseline to 18 months

  8. Low-density Lipoprotein (LDL)

    Whole blood will be drawn by a trained phlebotomist following a minimum 12-hr. fast and sent to The University of Kansas Health Systems for analysis.

    Time frame: Baseline to 18 months

  9. Fasting Glucose

    Whole blood will be drawn by a trained phlebotomist following a minimum 12-hr. fast and sent to The University of Kansas Health Systems for analysis.

    Time frame: Baseline to 18 months

  10. Hemoglobin A1c (HbA1c)

    Whole blood will be drawn by a trained phlebotomist following a minimum 12-hr. fast and sent to The University of Kansas Health Systems for analysis.

    Time frame: Baseline to 18 months

  11. Resting Blood Pressure

    Resting systolic and diastolic blood pressure will be measured on the non-dominant arm with participants seated in a chair and both feet flat on the ground.

    Time frame: Baseline to 18 months

  12. Cooking Skills

    Cooking skills will be assessed using the Assessment of Functional Living Skills (AFLS): Independent Living Skills. Scores range from 48 to 336, with a lower score indicating increased independence.

    Time frame: Baseline to 18 months

Other outcomes

  1. Skin Carotenoid Content

    We will assess skin carotenoid content with a finger scan using the Veggie Meter (Longevity Link Corporation), as biomarker of fruit and vegetables intake.

    Time frame: Baseline to 18 months

  2. Dietary Intake

    Dietary intake will be assessed using the NHANES Dietary Screener Questionnaire which is a 26 item questionnaire that asks about the past months consumption of fruits, vegetables, dairy, added sugars, whole grains, red meat and processed meat. Based on the self-reported consumption, values for average daily intake are provided.

    Time frame: Baseline to 18 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06961591
Responsible party
Sponsor
First posted
May 8, 2025
Start date
May 19, 2025
Primary completion
Dec 31, 2028 (estimated)
Completion
Jul 1, 2029 (estimated)
Last update
Aug 11, 2026

Study contacts

Lauren Ptomey, PhD
Contact
lptomey@kumc.edu
913-588-7983
Jessica Danon
Contact
jdanon@kumc.edu
785-764-3574

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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