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

Primary Purpose

PreDiabetes, Adult Children

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Metformin
Digital Intervention
Sponsored by
St. Jude Children's Research Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for PreDiabetes

Eligibility Criteria

18 Years - 44 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • St. Jude Children's Research HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment

Arm Description

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.

Outcomes

Primary Outcome Measures

Adherence for feasibility
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.
Digitally-delivered core education curriculum through the lifestyle change platform
Adherence will be monitored by completion logs of lessons
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Safety and Adverse Events (Symptom Log including monitoring for AEs)
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Drug adherence/Pill Counts
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.

Secondary Outcome Measures

Glycemic Control
Glycemic Control will be measured by Change in Hemoglobin A1c
Glycemic Control
Glycemic Control will be measure by Change in Fasting Plasma Glucose

Full Information

First Posted
January 6, 2021
Last Updated
August 28, 2023
Sponsor
St. Jude Children's Research Hospital
Collaborators
St. Baldrick's Foundation, Conquer Cancer Foundation, National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT04742751
Brief Title
An Open-Label Pilot Intervention Trial to Prevent Diabetes in Prediabetic Adult Survivors of Childhood Cancer
Official Title
An Open-Label Pilot Intervention Trial to Prevent Diabetes in Prediabetic Adult Survivors of Childhood Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 2, 2022 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
March 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Jude Children's Research Hospital
Collaborators
St. Baldrick's Foundation, Conquer Cancer Foundation, National Cancer Institute (NCI)

4. Oversight

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
Data Monitoring Committee
No

5. 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 (including a 12-week lifestyle alone run-in followed by 12-week combined intervention among survivors remaining prediabetic). 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.
Detailed Description
Eligible subjects who meet inclusion criteria will be enrolled in a 12 week run-in period of the digital lifestyle intervention program. At the 12 week study visit, those who remain prediabetic will received metformin extended release daily, first at lower dose (500 mg/day) to minimize gastrointestinal side effects (diarrhea, nausea, flatulence, bloating), then escalated to a maximum dose of 1000 mg/day at week 14. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes, Adult Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
The schema was changed the to an adaptive trial design with a 12 week lifestyle run-in followed by a combined metformin+lifestyle intervention for 12 weeks
Allocation
N/A
Enrollment
55 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
D-Care DM2, Fortamet, Glucophage, Glucophage XR, Glumetza, Riomet, Metformin ER
Intervention Description
To begin week 12 for participants who remain prediabetic after 12 week lifestyle run-in. Dosage and Route of Administration: 500 mg dose/ day to be taken orally, increased to 1000 mg dose/ day at week 14 through week 24. The dose should be taken immediately following the evening meal and at approximately the same time daily
Intervention Type
Behavioral
Intervention Name(s)
Digital Intervention
Other Intervention Name(s)
Lifestyle Change Digital Intervention
Intervention Description
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.
Primary Outcome Measure Information:
Title
Adherence for feasibility
Description
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.
Time Frame
2 years
Title
Digitally-delivered core education curriculum through the lifestyle change platform
Description
Adherence will be monitored by completion logs of lessons
Time Frame
At end of Week 24
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 4
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 8
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 12
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 14
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 16
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 20
Title
Safety and Adverse Events (Symptom Log including monitoring for AEs)
Description
An Adverse Event Monitoring Log with Global Rating of Side Effects Burden
Time Frame
Week 24
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 2
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 4
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 8
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 12
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 16
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 20
Title
Drug adherence/Pill Counts
Description
Adherence will be monitored by pill counts showing participant taking study drug, metformin ER, 80% of the time.
Time Frame
Week 24
Secondary Outcome Measure Information:
Title
Glycemic Control
Description
Glycemic Control will be measured by Change in Hemoglobin A1c
Time Frame
Baseline to Week 24 (on campus labs at Baseline, Week 12 and 24)
Title
Glycemic Control
Description
Glycemic Control will be measure by Change in Fasting Plasma Glucose
Time Frame
Baseline to Week 24 (on campus labs at Baseline, Week 12 and 24

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Investigators will recruit to enroll 55 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 105-125 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stephanie Dixon, MD, MPH
Phone
866-278-5833
Email
referralinfo@stjude.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephanie Dixon, MD, MPH
Organizational Affiliation
St. Jude Children's Research Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Jude Children's Research Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38105
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephanie Dixon, MD, MPH
Phone
866-278-5833
Email
referralinfo@stjude.org
First Name & Middle Initial & Last Name & Degree
Stephanie Dixon, MD, MPH

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing 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.
IPD Sharing Time Frame
Data will be made available at the time of article publication.
IPD Sharing 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.
Links:
URL
http://www.stjude.org
Description
St. Jude Children's Research Hospital
URL
http://www.tjude.org/protocols
Description
Clinical Trials Open at St. Jude

Learn more about this trial

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

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