An Open-Label Pilot Intervention Trial to Prevent Diabetes in Prediabetic Adult Survivors of Childhood Cancer

• ClinicalTrials.gov Identifier: NCT04742751
• Recruitment Status: Recruiting
• First Posted: February 8, 2021
• Last Update Posted: March 8, 2022
• Sponsor: St. Jude Children's Research Hospital
• Collaborator: St. Baldrick's Foundation
• Information provided by (Responsible Party): St. Jude Children's Research Hospital

Study Description

Brief Summary:

This is a first-in survivor, single-arm pilot study with the goal of establishing evidence of feasibility and safety of a combined pharmacologic (metformin) and lifestyle intervention (using an existing digital platform) to prevent diabetes in prediabetic adult survivors of childhood cancer.

Primary Objective

The primary aim of this proposal is to establish the feasibility and safety of a 24-week combined metformin + intensive lifestyle intervention among adult survivors with prediabetes.

Primary endpoints of this trial will be adherence to 1) daily metformin administration and 2) completion of required core-curriculum of the lifestyle change intervention. Safety will be assessed using the Global Rating of Side Effects Burden

Secondary Objectives

The secondary aim is to assess preliminary evidence for efficacy of the combined metformin + intensive lifestyle intervention on glycemic control and insulin resistance. Glycemic control will be measured by fasting plasma glucose (FPG) and hemoglobin A1c (HbA1c) and insulin resistance measured by the homeostatic model assessment (HOMA-IR) and IGF- binding protein 1 (IGF-BP1; a measure of insulin sensitivity strongly correlated with euglycemic insulin clamp testing).

Exploratory Objectives

To assess preliminary evidence for efficacy of the combined metformin + intensive lifestyle intervention on weight, other anthropometric measures, blood pressure and lipid profile, physical activity (self-reported and as measured by accelerometer), frailty measures, and health-related quality of life (HRQOL). We will also assess diabetes development at future SJLIFE visits.

To assess measures of participation in the lifestyle change program as well as barriers to participation and medication adherence.

Condition or disease	Intervention/treatment	Phase
PreDiabetes; Adult Children	Drug: Metformin; Behavioral: Digital Intervention	Phase 2

Detailed Description:

Eligible subjects who meet inclusion criteria will receive metformin extended release daily and be enrolled in the digital lifestyle intervention program. Following a 2-week run-in period at lower dose (500 mg/day) to minimize gastrointestinal side effects (diarrhea, nausea, flatulence, bloating), participants will be escalated to a maximum dose of 1000 mg/day. The digitally delivered lifestyle change program will include a core curriculum focused on diet quality, food types, exercise and behavioral strategies for goal setting, and self-monitoring.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 41 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: An Open-Label Pilot Intervention Trial to Prevent Diabetes in Prediabetic Adult Survivors of Childhood Cancer
• Actual Study Start Date: March 2, 2022
• Estimated Primary Completion Date: March 2024
• Estimated Study Completion Date: March 2025

Arms and Interventions

Arm

Intervention/treatment

Experimental: Treatment; Metformin is an antihyperglycemic agent which improves glucose tolerance in patients with type 2 diabetes mellitus, lowering both basal and postprandial plasma glucose. Metformin decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. With Metformin therapy, insulin secretion remains unchanged while fasting insulin levels and day-long plasma insulin response may decrease.

Drug: Metformin; Dosage and Route of Administration: 500 mg dose/day to be taken orally, increased to 1000 mg dose/day at day 14 through week 24. The dose should be taken immediately following the evening meal and at approximately the same time daily; Other Names: D-Care DM2; Fortamet; Glucophage; Glucophage XR; Glumetza; Riomet; Metformin ER; Behavioral: Digital Intervention; Lifestyle Change Digital Intervention - This is a digital platform that will include a core curriculum focused on diet, exercise, and behavioral strategies for goal setting and self-monitoring to improve diet including a weight loss On Day 1, participants will begin their digital lifestyle intervention using their smart-phone application with their lifestyle coach and peer group. On day 14, participants will be contacted by phone (+/- 4 days, day 10 to 18) and adherence assessed using virtual pill counts via phone calls. At weeks 4, 8, 16 and 20 a phone-based pill count for adherence and adverse event symptom log will be completed and study medication dispensed. At week 12 (interim assessment) and 24 (study-end), the participant will return to St. Jude Children's Research Hospital (SJCRH) for an in-person assessment. The digital lifestyle change program will complete at week 24.; Other Name: Lifestyle Change Digital Intervention

Outcome Measures

Primary Outcome Measures :

1. Adherence for feasibility [ Time Frame: 2 years ]
   Adherence to the intervention with 80% adherence to prescribed metformin and completion of 60% of the digitally-delivered core education curriculum through the lifestyle change platform.
2. Digitally-delivered core education curriculum through the lifestyle change platform [ Time Frame: At end of Week 24 ]
   Adherence will be monitored by completion logs of lessons
3. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 2 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
4. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 4 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
5. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 8 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
6. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 12 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
7. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 16 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
8. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 20 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
9. Safety and Adverse Events (Symptom Log including monitoring for AEs) [ Time Frame: Week 24 ]
   An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
10. Drug adherence/Pill Counts [ Time Frame: Week 2 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
11. Drug adherence/Pill Counts [ Time Frame: Week 4 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
12. Drug adherence/Pill Counts [ Time Frame: Week 8 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
13. Drug adherence/Pill Counts [ Time Frame: Week 12 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
14. Drug adherence/Pill Counts [ Time Frame: Week 16 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
15. Drug adherence/Pill Counts [ Time Frame: Week 20 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
16. Drug adherence/Pill Counts [ Time Frame: Week 24 ]
    Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.

Secondary Outcome Measures :

1. Glycemic Control [ Time Frame: Baseline to Week 24 (on campus labs at Baseline, Week 12 and 24) ]
   Glycemic Control will be measured by Change in Hemoglobin A1c
2. Glycemic Control [ Time Frame: Baseline to Week 24 (on campus labs at Baseline, Week 12 and 24 ]
   Glycemic Control will be measure by Change in Fasting Plasma Glucose

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 44 Years (Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Investigators will recruit to enroll 41 survivors who are at least 18 but <45 years of age who participate in the St. Jude Lifetime Cohort Study (SJLIFE) and have been identified to have prediabetes defined as hemoglobin A1c (HbA1c)
• Participant in SJLIFE
• ≥18 and <45 years of age
• Prediabetic: fasting plasma glucose 100-125 mg/dL, hemoglobin A1c 5.7- 6.4% (either or both criteria may be present) According to institutional and NIH policy, the study will accession research participants regardless of sex and ethnic background. Institutional experience confirms broad representation in this regard.

Exclusion Criteria:

• Absence of treatment related diabetes risk. Survivors will be excluded if their cancer treatment required observation only, surgery alone not involving the abdomen or brain, radiation alone not involving the chest (pancreatic risk), abdomen or brain (e.g. retinoblastoma treated with enucleation alone, melanoma of an extremity treated with excision alone, neuroblastoma in an infant requiring observation only)
• Diabetes at baseline assessment: FPG ≥126 mg/dL, HbA1c ≥6.5% or previous diagnosis by a physician (except gestational diabetes that resolved post-partum)
• BMI <19 kg/m2
• Current metformin use (including for any period ≥30 days in the past 1yr)
• Known allergy to metformin
• Current use of other oral glucose lowering medications, non-insulin injectable diabetes medications or insulin (Appendix)
• Current participation in a lifestyle change program
• Chronic kidney disease ≥ stage IIIb (eGFR < 45 mL/min)
• Severe cardiovascular disease or recent intervention (NYHA class ≥2 or heart failure hospitalization in the past 6mo, Aortic stenosis, Heart block including LBBB or 3rd degree AV block, SBP >180 or DBP >105 mmHg, myocardial infarction or coronary revascularization in the past 1 month)
• Severe hepatic dysfunction: cirrhosis or AST/ALT >3 times upper limit of normal
• Pulmonary disease with dependence on oxygen or daily use of bronchodilators
• Weight loss >10% in the past 6 months
• Bariatric surgery in the past 2 years
• Pregnant, within 3 months post-partum, nursing, or planning to become pregnant
• Anemia: hematocrit <36% in males or <33% in females
• Ongoing alcohol or substance abuse using criteria from the AUDIT and DAST questionnaires (Appendix)
• Diagnosis of schizophrenia or other psychotic disorder
• Vision impairment limiting ability to interface with the digital program
• Unable to swallow medication
• Non-English speaking
• Cognitive impairment defined by IQ <80
• Current active cancer or undergoing treatment for active cancer

Contacts and Locations

Contacts

Contact: Stephanie Dixon, MD, MPH; 866-278-5833; referralinfo@stjude.org

Locations

United States, Tennessee

St. Jude Children's Research Hospital; Recruiting

Memphis, Tennessee, United States, 38105

Contact: Stephanie Dixon, MD, MPH 866-278-5833 referralinfo@stjude.org

Principal Investigator: Stephanie Dixon, MD, MPH

Sponsors and Collaborators

St. Jude Children's Research Hospital

St. Baldrick's Foundation

Investigators

• Principal Investigator: Stephanie Dixon, MD, MPH; St. Jude Children's Research Hospital

  Study Documents (Full-Text)

Documents provided by St. Jude Children's Research Hospital:

Study Protocol and Statistical Analysis Plan  [PDF] November 10, 2020

More Information

Additional Information:

St. Jude Children's Research Hospital 

Clinical Trials Open at St. Jude 

• Responsible Party: St. Jude Children's Research Hospital
• ClinicalTrials.gov Identifier: NCT04742751
• Other Study ID Numbers: PREDM
• First Posted: February 8, 2021
• Last Update Posted: March 8, 2022
• Last Verified: March 2022

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: Yes
• Plan Description: Individual participant de-identified datasets containing the variables analyzed in the published article will be made available (related to the study primary or secondary objectives contained in the publication). Supporting documents such as the protocol, statistical analyses plan, and informed consent are available through the CTG website for the specific study. Data used to generate the published article will be made available at the time of article publication. Investigators who seek access to individual level de-identified data will contact the computing team in the Department of Biostatistics (ClinTrialDataRequest@stjude.org) who will respond to the data request.
• Supporting Materials: Study Protocol; Statistical Analysis Plan (SAP); Informed Consent Form (ICF)
• Time Frame: Data will be made available at the time of article publication.
• Access Criteria: Data will be provided to researchers following a formal request with the following information: full name of requestor, affiliation, data set requested, and timing of when data is needed. As an informational point, the lead statistician and study principal investigator will be informed that primary results datasets have been requested.

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Product Manufactured in and Exported from the U.S.: No

Additional relevant MeSH terms:

Prediabetic State; Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Metformin; Hypoglycemic Agents; Physiological Effects of Drugs