A Pilot Study of a Low Glycemic Load Diet in Adults With Cystic Fibrosis
Primary Purpose
Cystic Fibrosis, Cystic Fibrosis-related Diabetes, Cystic Fibrosis With Intestinal Manifestations
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Low Glycemic Load Diet
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic Fibrosis Related Diabetes, Low Glycemic Load, Continuous Glucose Monitoring
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of CF
- Diagnosis of pancreatic insufficiency, requiring pancreatic enzyme replacement
- Oral glucose tolerance test within the past three years showing impaired glucose tolerance (2-hour glucose ≥140 mg/dL) or indeterminate glycemia (1-hour glucose ≥200), HbA1c 5.7-6.4% in the past one year, and/or or documented random glucose ≥200 in the past one year
- BMI 21-25 kg/m2
- 18 years and above
Exclusion Criteria:
- Current use of insulin
- Most recent HbA1c ≥6.5%
- History of solid organ transplant or currently listed for solid organ transplant
- FEV1 <50% predicted on most recent pulmonary function testing
- Currently receiving enteral nutrition support
- Current or anticipated pregnancy in the next 1 year
- Hospitalization for CF exacerbation within 1 month of enrollment
- Started or stopped treatment with Trikafta or other CFTR modulator within 3 months of enrollment
- Currently adhering to a low glycemic index or other carbohydrate restricted diet
Sites / Locations
- Boston Children's Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Low Glycemic Load Diet
Arm Description
Feeding study with dietary composition (approximately) 50% fat, 30% carbohydrate, 20% protein.
Outcomes
Primary Outcome Measures
Change in weight from baseline and 10 weeks
Anthropometric measure
Change in percent time <54 mg/dL
Continuous glucose monitoring
Patient reported tolerability of dietary intervention, Likert scale
Single Likert scale question of overall diet tolerability, ranging from 1 (intolerable) to 10 (completely tolerable)
Secondary Outcome Measures
Change in percent time >140 mg/dL
Continuous glucose monitoring
Change in CGM average glucose
Continuous glucose monitoring
Change in CGM glucose management indicator (GMI)
Continuous glucose monitoring
Change in CGM standard deviation (SD)
Continuous glucose monitoring
Change in CGM coefficient of variation (CV)
Continuous glucose monitoring
Change in percent time less than 50 mg/dL on CGM
Continuous glucose monitoring
Change in percent time less than 70 mg/dL on CGM
Continuous glucose monitoring
Change in percent time 70-180 mg/dL on CGM
Continuous glucose monitoring
Change in percent time greater than 180 mg/dL on CGM
Continuous glucose monitoring
Change in percent time greater than >250 mg/dL on CGM
Continuous glucose monitoring
Number of episodes of symptomatic hypoglycemia
Survey
Change in lean and fat mass
DXA body composition measures
Change in Patient Assessment of Constipation (PAC) questionnaire score
Likert scale questionnaire with 12 items, each item scored 0-4, total score ranging from 0-48 with higher scores related to worse outcomes
Change in Patient Assessment of Gastrointestinal Symptom (PAGI-SYM) questionnaire score
Likert scale questionnaire with 20 items, each item scored 0-5, total score ranging from 0-100 with higher scores related to worse outcomes
Change in Modified Activity Questionnaire (MAQ) score
Questionnaire, units of total hours of exercise over past 12 months, no min or max scores, higher value related to better outcome
Change in Cystic Fibrosis Questionnaire Revised (CFQ-R) score
Likert scale questionnaire, 50 items, each scored 0-4, total score ranging from 0-100 with higher value reflecting better outcome
Change in erythrocyte sedimentation rate (ESR)
Laboratory test, measured in mm/hr
Change in c-reactive protein (CRP)
Laboratory test, measured in mg/L
Change in intestinal fatty acid binding protein (I-FABP)
Laboratory test, measured in ng/mL
Full Information
NCT ID
NCT04519853
First Posted
July 7, 2020
Last Updated
August 9, 2023
Sponsor
Boston Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04519853
Brief Title
A Pilot Study of a Low Glycemic Load Diet in Adults With Cystic Fibrosis
Official Title
A Pilot Study to Test the Safety and Tolerability of a Low Glycemic Load Dietary Intervention in Adults With Cystic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
October 25, 2021 (Actual)
Primary Completion Date
July 1, 2023 (Actual)
Study Completion Date
July 1, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Children's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This pilot study will evaluate the safety and tolerability of a low glycemic load dietary intervention in adult patients with cystic fibrosis (CF) in a rigorous feeding study. Specific emphasis will be placed on changes in weight, body composition, and glycemic measures obtained via continuous glucose monitor (CGM) usage.
Detailed Description
Non-pulmonary complications of cystic fibrosis (CF) are becoming increasingly prevalent with the changing landscape of CF care. CF related diabetes mellitus (CFRD) and CF related gastrointestinal (GI) complications have significant effects on morbidity and mortality. Treatment options are limited to insulin therapy for CFRD and symptom control for most GI complications.
BMI is a well-established marker of morbidity and mortality in patients with CF. Many patients consume a high carbohydrate intake to meet their increase caloric needs, potentially leading to complications including post-prandial hyperglycemia, increased inflammation, and abnormal GI motility. Dietary recommendations for children and adults with CF are limited and based entirely on consensus and expert opinion. As patients with CF live longer with highly effective modulator therapy, it is important to understand the effects of dietary composition on short and long-term endocrine, GI, and pulmonary outcomes.
The investigators will conduct a prospective, open-label pilot study in adults with CF and impaired glucose tolerance or indeterminate glycemia to establish the safety and tolerability of a low glycemic load (LGL) diet. Subjects will initially follow their standard diet for a 2-week run-in period, then transition to a LGL diet provided by a food delivery service for the remaining 8 weeks. The investigators will also investigate potential short-term outcomes of dietary carbohydrate manipulation, including glycemic variability measured by continuous glucose monitor (CGM), body composition via DXA, GI symptoms, and quality of life measures.
The investigators hypothesize that a diet lower in carbohydrate content will be safe, tolerable, and associated with weight maintenance or gain, and that a LGL diet will result in decreased glycemic variability via CGM, improved GI symptoms, increased lean to fat mass ratio, and improved quality of life measures over an 8-week period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Cystic Fibrosis-related Diabetes, Cystic Fibrosis With Intestinal Manifestations
Keywords
Cystic Fibrosis Related Diabetes, Low Glycemic Load, Continuous Glucose Monitoring
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single dietary treatment arm with run-in period as a control
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Low Glycemic Load Diet
Arm Type
Experimental
Arm Description
Feeding study with dietary composition (approximately) 50% fat, 30% carbohydrate, 20% protein.
Intervention Type
Behavioral
Intervention Name(s)
Low Glycemic Load Diet
Intervention Description
Food delivery service will provide a low glycemic load diet for 8 weeks
Primary Outcome Measure Information:
Title
Change in weight from baseline and 10 weeks
Description
Anthropometric measure
Time Frame
Baseline and 10 weeks
Title
Change in percent time <54 mg/dL
Description
Continuous glucose monitoring
Time Frame
Baseline and 10 weeks
Title
Patient reported tolerability of dietary intervention, Likert scale
Description
Single Likert scale question of overall diet tolerability, ranging from 1 (intolerable) to 10 (completely tolerable)
Time Frame
Single measurement at 10 weeks after diet completion
Secondary Outcome Measure Information:
Title
Change in percent time >140 mg/dL
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in CGM average glucose
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in CGM glucose management indicator (GMI)
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in CGM standard deviation (SD)
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in CGM coefficient of variation (CV)
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in percent time less than 50 mg/dL on CGM
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in percent time less than 70 mg/dL on CGM
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in percent time 70-180 mg/dL on CGM
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in percent time greater than 180 mg/dL on CGM
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Change in percent time greater than >250 mg/dL on CGM
Description
Continuous glucose monitoring
Time Frame
Baseline to 10 weeks
Title
Number of episodes of symptomatic hypoglycemia
Description
Survey
Time Frame
Baseline and 10 weeks
Title
Change in lean and fat mass
Description
DXA body composition measures
Time Frame
Baseline and 10 weeks
Title
Change in Patient Assessment of Constipation (PAC) questionnaire score
Description
Likert scale questionnaire with 12 items, each item scored 0-4, total score ranging from 0-48 with higher scores related to worse outcomes
Time Frame
Baseline and 10 weeks
Title
Change in Patient Assessment of Gastrointestinal Symptom (PAGI-SYM) questionnaire score
Description
Likert scale questionnaire with 20 items, each item scored 0-5, total score ranging from 0-100 with higher scores related to worse outcomes
Time Frame
Baseline and 10 weeks
Title
Change in Modified Activity Questionnaire (MAQ) score
Description
Questionnaire, units of total hours of exercise over past 12 months, no min or max scores, higher value related to better outcome
Time Frame
Baseline and 10 weeks
Title
Change in Cystic Fibrosis Questionnaire Revised (CFQ-R) score
Description
Likert scale questionnaire, 50 items, each scored 0-4, total score ranging from 0-100 with higher value reflecting better outcome
Time Frame
Baseline and 10 weeks
Title
Change in erythrocyte sedimentation rate (ESR)
Description
Laboratory test, measured in mm/hr
Time Frame
Baseline and 10 weeks
Title
Change in c-reactive protein (CRP)
Description
Laboratory test, measured in mg/L
Time Frame
Baseline and 10 weeks
Title
Change in intestinal fatty acid binding protein (I-FABP)
Description
Laboratory test, measured in ng/mL
Time Frame
Baseline and 10 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of CF
Diagnosis of pancreatic insufficiency, requiring pancreatic enzyme replacement
Oral glucose tolerance test within the past three years showing impaired glucose tolerance (2-hour glucose ≥140 mg/dL) or indeterminate glycemia (1-hour glucose ≥200), HbA1c 5.7-6.4% in the past one year, and/or or documented random glucose ≥200 in the past one year
BMI 21-25 kg/m2
18 years and above
Exclusion Criteria:
Current use of insulin
Most recent HbA1c ≥6.5%
History of solid organ transplant or currently listed for solid organ transplant
FEV1 <50% predicted on most recent pulmonary function testing
Currently receiving enteral nutrition support
Current or anticipated pregnancy in the next 1 year
Hospitalization for CF exacerbation within 1 month of enrollment
Started or stopped treatment with Trikafta or other CFTR modulator within 3 months of enrollment
Currently adhering to a low glycemic index or other carbohydrate restricted diet
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Melissa S Putman, MD,MS
Organizational Affiliation
Boston Children's Hospital; Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston Children's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share IPD data with other researchers.
Citations:
PubMed Identifier
21115772
Citation
Moran A, Brunzell C, Cohen RC, Katz M, Marshall BC, Onady G, Robinson KA, Sabadosa KA, Stecenko A, Slovis B; CFRD Guidelines Committee. Clinical care guidelines for cystic fibrosis-related diabetes: a position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society. Diabetes Care. 2010 Dec;33(12):2697-708. doi: 10.2337/dc10-1768. No abstract available.
Results Reference
background
PubMed Identifier
31659728
Citation
Gabel ME, Galante GJ, Freedman SD. Gastrointestinal and Hepatobiliary Disease in Cystic Fibrosis. Semin Respir Crit Care Med. 2019 Dec;40(6):825-841. doi: 10.1055/s-0039-1697591. Epub 2019 Oct 28.
Results Reference
background
PubMed Identifier
31036487
Citation
Prentice BJ, Ooi CY, Strachan RE, Hameed S, Ebrahimkhani S, Waters SA, Verge CF, Widger J. Early glucose abnormalities are associated with pulmonary inflammation in young children with cystic fibrosis. J Cyst Fibros. 2019 Nov;18(6):869-873. doi: 10.1016/j.jcf.2019.03.010. Epub 2019 Apr 26.
Results Reference
background
PubMed Identifier
16844431
Citation
Brennan AL, Gyi KM, Wood DM, Johnson J, Holliman R, Baines DL, Philips BJ, Geddes DM, Hodson ME, Baker EH. Airway glucose concentrations and effect on growth of respiratory pathogens in cystic fibrosis. J Cyst Fibros. 2007 Apr;6(2):101-9. doi: 10.1016/j.jcf.2006.03.009. Epub 2006 Jul 17.
Results Reference
background
PubMed Identifier
22606371
Citation
Balzer BW, Graham CL, Craig ME, Selvadurai H, Donaghue KC, Brand-Miller JC, Steinbeck KS. Low glycaemic index dietary interventions in youth with cystic fibrosis: a systematic review and discussion of the clinical implications. Nutrients. 2012 Apr;4(4):286-96. doi: 10.3390/nu4040286. Epub 2012 Apr 18.
Results Reference
background
Links:
URL
https://www.cff.org/sites/default/files/2021-11/Patient-Registry-Annual-Data-Report.pdf
Description
CFF 2021 Patient Registry Annual Data Report
Learn more about this trial
A Pilot Study of a Low Glycemic Load Diet in Adults With Cystic Fibrosis
We'll reach out to this number within 24 hrs