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NCT Number: NCT05723445

The Effects of a Low Glycemic Load Diet on Dysglycemia and Body Composition in Adults With Cystic Fibrosis-Related Diabetes

This study will evalute the effect of a low glycemic load (LGL diet on dysglycemia, insulin requirements, DXA-derived body composition, gastrointestinal symptoms and quality of life measures in adults with cystic fibrosis-related diabetes (CFRD). We will use continuous glucose monitors (CGM) to assess the LGL diet both in a controlled setting (via a meal delivery company) and in free-living conditions.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Boston Children's Hospital, Boston, Massachusetts, United States

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About this study

Maintenance of a healthy body mass index (BMI) is a well-established marker of improved morbidity and mortality in patients with cystic fibrosis (CF). To achieve and maintain adequate weight, patients with CF are encouraged to consume a caloric intake of 120-150% of the dietary reference intake (DRI) for the typical healthy adult. However, dietary recommendations for children and adults with CF are based entirely on consensus and expert opinion. High carbohydrate intake is typical for patients with CF, but this may lead to multiple complications including post-prandial hyperglycemia, increased inflammation, and abnormal GI motility and may predispose to obesity and metabolic syndrome. Dietary changes are a commonly used treatment approach for CF-related diabetes (CFRD), despite the fact that there are no data establishing whether dietary interventions are helpful in preventing and/or treating CFRD. Particularly as patients with CF live longer with highly effective modulator therapy and as the prevalence of cardiovascular and metabolic disease increases in this population, it is crucial to understand the effects of dietary composition on short and long-term endocrine, GI, and pulmonary outcomes.

In patients with both type 1 and type 2 diabetes mellitus, a low glycemic load (LGL) diet has been shown to improve glycemic variability, A1c level, insulin sensitivity, and quality of life without increasing hypoglycemic events. Significant glycemic variability is associated with increased markers of inflammation in adolescents with T1DM, possibly serving as a mechanistic link to the development of cardiovascular disease. Particularly as rates of obesity and cardiovascular disease continue to increase, this diet may be particularly useful in patients with CF, altered glucose homeostasis, and/or obesity. There are currently no prospective studies evaluating the impact of diet quality on glycemic control and body composition in patients with CF. The gold standard approach for assessing the safety and efficacy of dietary interventions is a food delivery study.

The investigators will conduct a prospective, open-label study in adults with CFRD to determine the effects of an LGL diet on dysglycemia and body composition. Participants will initially follow their standard diet for a 10-day run-in period. They will then transition to an LGL diet provided by a meal delivery company for 8 weeks. During this period, they will wear a continuous glucose monitor (CGM) for 2 10-day periods. Finally, participants will adhere to an LGL diet under free-living conditions with close nutritionist follow-up for a period of 4 months. Serum studies, DXA-body composition, anthropometric data, GI symptoms and quality of life measures will be obtained at baseline, after the meal-delivery phase and at study completion.

The investigators hypothesize that an LGL diet will result in improved CGM-derived measures of hyperglycemia, a decrease in insulin requirements, and reductions in fat-mass index on DXA analysis in adults with CFRD over an 8-week period during a meal delivery period. Furthermore, they hypothesize that these changes will be sustainable under free-living conditions during a 4-month period.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18 years and above
  • Genetically confirmed diagnosis of CF
  • Diagnosis of pancreatic insufficiency, requiring pancreatic enzyme replacement
  • Criteria for CFRD:

A.) Most recent OGTT 2-hour glucose >200 mg/dL within the past two years, and/or; B.) HbA1c >6.5% in the past two years, and/or; C.) Current use of insulin

Exclusion criteria

  • FEV1 <50% predicted on most recent pulmonary function testing
  • BMI <18 kg/m2
  • Currently receiving enteral nutrition support via GT feeds
  • Pregnancy, plan to become pregnant in the next 3-months, or sexually active without use of contraception
  • Use of IV antibiotics or systemic supraphysiologic glucocorticoids for CF exacerbation within 1 month
  • Started or stopped treatment with a CFTR modulator within 3 months of enrollment
  • Currently adhering to an LGL or other carbohydrate-restricted diet (carbohydrate intake <30% of total daily caloric intake)

Treatment and study plan

Low Glycemic Load diet

Behavioral

Food delivery service will provide a low glycemic load diet for 8 weeks, followed by a 4-month period of self-adherence to a low glycemic load diet with close nutritionist follow up

Primary outcomes

  1. Change in percent time in target range 70-180 mg/dL

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

Secondary outcomes

  1. Change in CGM average glucose (AG) mg/dL

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  2. Change in percent time >180 mg/dL

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  3. Change in percent time >250 mg/dL

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  4. Change in CGM standard deviation (SD)

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  5. Change in CGM coefficient of variation (CV)

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  6. Change in percent time <70 mg/dL

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  7. Change in percent time <54 mg/dL

    Time frame: Baseline, post-meal delivery phase (8 weeks), post-free-living conditions phase (4 months)

    Continuous glucose monitoring

  8. Change in number of episodes of symptomatic hypoglycemia (average per week)

    Time frame: Baseline (weeks 1-2), visit 2 (post-meal delivery phase, weeks 2-10), visit 3 (post-free living conditions phase, weeks 11-26))

    Weekly emailed survey

  9. Change in total daily dose of insulin (TDD)

    Time frame: Baseline (weeks 1-2), visit 2 (post-meal delivery phase, weeks 2-10), visit 3 (post-free living conditions phase, weeks 11-26)

    Weekly emailed survey

  10. Change in body mass index (BMI, kg/m2)

    Time frame: Baseline (weeks 1-2), visit 2 (post-meal delivery phase, weeks 2-10), visit 3 (post-free living conditions phase, weeks 11-26)

    Every other week emailed survey

  11. Change in weight (kg)

    Time frame: Baseline (weeks 1-2), visit 2 (post-meal delivery phase, weeks 2-10), visit 3 (post-free living conditions phase, weeks 11-26)

    Every other week emailed survey

  12. Change fat-mass index (FMI, fat mass kg/ height m^2)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    DXA body composition measures

  13. Change in percent body fat (%)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    DXA body composition measures

  14. Change in appendicular lean mass index (ALMI, lean mass kg/ height m^2)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    DXA body composition measures

  15. Change in Patient Assessment of Constipation (PAC) questionnaire score

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Likert scale questionnaire with 12 items, each scored 0-4, total score ranging from 0-48 with higher scores related to worse outcomes

  16. Change in Patient Assessment of Gastrointestinal Symptoms (PAGI-Sym) questionnaire score

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Likert scale questionnaire with 20 items, each scored 0-5, total score ranging from 0-100 with higher scores related to worse outcomes

  17. Change in Cystic Fibrosis Questionnaire Revised (CFQ-R) score

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Likert scale questionnaire with 50 items, each scored 0-4, total score ranging from 0-100 with higher scores reflecting better outcomes

  18. Change in Diet Tolerability Questionnaire

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Likert scale questionnaire with 5 items, each scored 0-10, total score ranging from 0-50 with higher scores reflecting better diet tolerability

  19. Change in Bristol stool chart data

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Chart depicting 7 types of stool patterns, ranging from constipation to diarrhea

  20. Change in erythrocyte sedimentation rate (ESR)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in mm/hr

  21. Change in c-reactive protein (CRP)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in mg/L

  22. Change in hemoglobin A1c

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in %

  23. Change in total cholesterol

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in mg/dL

  24. Change in high-density lipoprotein (HDL)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in mg/dL

  25. Change in low-density lipoprotein (LDL)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in mg/dL

  26. Change in triglyceride level

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in mg/dL

  27. Change in intestinal fatty acid binding protein (I-FABP)

    Time frame: Baseline (week 1), visit 2 (post-meal delivery phase, week10), visit 3 (post-free living conditions phase, week 26)

    Laboratory test, measured in ng/mL

Study contacts

Contact information is provided by the study sponsor or research team.

Kevin J Scully, MB BCh BAO

CONTACT

[email protected]

401-444-5504

Melissa S Putman, MD, MSc

CONTACT

[email protected]

617-355-7476

Sponsors and collaborators

Lead sponsor

Rhode Island Hospital

Other

Collaborators

  • Cystic Fibrosis Foundation

Registry information

Acronym: DINE

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Feb 10, 2023
Registry last updated
Aug 22, 2025

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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