search
Back to results

Alcohol & Metabolic Comorbidities in PLWHA: Evidence Driven Interventions (ALIVE-Ex)

Primary Purpose

HIV/AIDS, Dysglycemia, Alcohol Use Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise
Sponsored by
Louisiana State University Health Sciences Center in New Orleans
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV/AIDS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. HIV positive
  2. Fasting glucose above 94 mg/dL and below 125 mg/dl
  3. Without diagnosis of diabetes mellitus
  4. "No" response to six questions in Physical Activity Readiness Questionnaire (PAR-Q), given at time of screening

Exclusion Criteria:

  1. Lack of informed consent
  2. Decisionally impaired individuals
  3. Non-English speaking
  4. Acute illness within the preceding six weeks (defined as fever, new antibiotic use or unscheduled healthcare visit (for illness))
  5. Acute alcohol intoxication
  6. Pregnancy
  7. Currently prescribed blood thinners (if undergoing muscle biopsy)
  8. Allergy to Lidocaine (if undergoing muscle biopsy)
  9. Significant peripheral neuropathies (if undergoing exercise)
  10. Significant cardiovascular impairments (if undergoing exercise)

Sites / Locations

  • Louisiana State University Health Sciences Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Exercise

Arm Description

Aerobic exercise program using treadmill.

Outcomes

Primary Outcome Measures

Fasting plasma glucose and OGTT values (subclinical dysglycemia)
Risk for subclinical dysglycemia

Secondary Outcome Measures

Skeletal muscle phenotype
Subclinical dysglycemia associated with dysfunctional skeletal muscle measured by myomiRs
Fasting plasma glucose
Glycemic control measured by fasting plasma glucose
myomiRs
Dysfunctional SKM measured by myomiRs

Full Information

First Posted
September 27, 2017
Last Updated
October 2, 2023
Sponsor
Louisiana State University Health Sciences Center in New Orleans
search

1. Study Identification

Unique Protocol Identification Number
NCT03299205
Brief Title
Alcohol & Metabolic Comorbidities in PLWHA: Evidence Driven Interventions
Acronym
ALIVE-Ex
Official Title
Alcohol & Metabolic Comorbidities in PLWHA: Evidence Driven Interventions
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
November 20, 2017 (Actual)
Primary Completion Date
September 15, 2023 (Actual)
Study Completion Date
September 15, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Louisiana State University Health Sciences Center in New Orleans

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Cross-sectional and prospective studies are proposed to test the prediction that a higher proportion of HIV+ individuals with hazardous alcohol drinking with subclinical fasting dysglycemia will present with impaired oral glucose tolerance and dysfunctional metabolic skeletal muscle phenotype. Prospective studies will test the efficacy of an exercise intervention in improving glycemic control. Results will inform larger scale interventions to ameliorate metabolic comorbidities, improve health, quality of life, and possibly decrease hazardous alcohol drinking.
Detailed Description
Adult male and female in care PLWHA with fasting plasma glucose (FPG) >94 mg/dL and <125 mg/dL will be recruited. Measures of FPG and HbA1c obtained from overnight fasted subjects. Alcohol use disorder (AUD) will be assessed by AUDIT and time-line follow back questionnaires, coupled with Phosphatidylethanol (PEth) measures. Glucose tolerance will be assessed by oral glucose tolerance test (OGTT). Blood sample collected at the time of the OGTT will be used for determination of circulating levels of adipokines (adiponectin and resistin). A subset of adult male and female PLWHA +/- AUD with impaired OGTT will be recruited to undergo skeletal muscle (SKM) biopsy (vastus lateralis), 90 min after a defined (calorie and nutrient composition) meal (i.e.,Ensure, Carnation Instant Breakfast). Muscle samples will be used for phenotype characterization (markers of inflammation, insulin signaling, mitochondrial homeostasis) and for myoblast isolation. Adult male and female PLWHA +/- AUD with impaired OGTT will undergo a moderate intensity aerobic exercise intervention that will include the wearing of an accelerometer (i.e. Fitbit Zip) to monitor daily activity and steps. A SKM biopsy will be performed after completion of the exercise protocol in a subset of subjects to examine the changes in gene expression and myoblast mitochondrial oxidative capacity. We will expand recruitment by enrolling PLWHA +/- AUD based on a FPG between 94-120 mg/dL to participate in the exercise intervention. Clearance for participation in this study will require EKG, completion of a physical activity readiness questionnaire, and medical clearance from a staff clinician. Individuals with significant peripheral neuropathies or the prevalence of significant cardiovascular impairments (i.e. resting cardiac abnormalities or arrhythmias, severe hypertension, etc.) will be excluded from exercise testing or intervention. The 10-week exercise intervention program will consist of aerobic exercise 3 days per week of moderate intensity for 30-45 minutes each session with the goal of achieving 135 minutes per week. The program will begin at low-moderate intensity (40 to 50% of heart rate reserve; HRR) and progress to a higher intensity (50 to 60% HRR) exercise after week 4 of the program. The frequency and duration of exercise sessions will remain constant after week 4 so the absolute dose of exercise will be altered through increasing intensity, i.e. from low-moderate to more vigorous. All exercise will be completed on a treadmill at the Louisiana State University Health Sciences Center (LSUHSC) Wellness Center. Additionally, each participant will be provided with a Fitbit Zip to monitor daily activity and steps. Data from the Fitbit Zip will be downloaded weekly basis. Participants will be given a healthy step goal of 7000 steps per day. Based on initial step counts after the first week of wearing the accelerometer, individual goals will be discussed with the participants. Personal limitations that develop during the study period (i.e. peripheral neuropathy, orthopedic limitation, etc.) will be monitored and will be reason for exclusion from the exercise program. All sessions will be supervised and adherence to the exercise prescription will be fully monitored under the supervision and care of Dr. Stefany Primeaux in consultation with Dr. Neil Johannsen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS, Dysglycemia, Alcohol Use Disorder

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
68 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise
Arm Type
Experimental
Arm Description
Aerobic exercise program using treadmill.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
The exercise intervention consists of moderate intensity aerobic exercise intervention that will include the wearing of an accelerometer (i.e. Fitbit Zip) to monitor daily activity and steps. Aerobic exercise will be conducted over 10-weeks in PLWHA +/- AUD. The programs will consist of aerobic exercise 3 days per week of moderate intensity for 30-45 minutes each session with the goal of achieving 135 minutes per week. The program will begin at low-moderate intensity and progress to higher intensity exercise after week 4 of the program. All exercise will be completed on a treadmill and supervised by study staff. Each participant will be provided with a Fitbit Zip to monitor daily activity and steps with a goal of 7000 steps per day.
Primary Outcome Measure Information:
Title
Fasting plasma glucose and OGTT values (subclinical dysglycemia)
Description
Risk for subclinical dysglycemia
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Skeletal muscle phenotype
Description
Subclinical dysglycemia associated with dysfunctional skeletal muscle measured by myomiRs
Time Frame
Baseline
Title
Fasting plasma glucose
Description
Glycemic control measured by fasting plasma glucose
Time Frame
Change from baseline in fasting plasma glucose after 10 weeks
Title
myomiRs
Description
Dysfunctional SKM measured by myomiRs
Time Frame
Change from baseline in myomiRs after 10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV positive Fasting glucose above 94 mg/dL and below 125 mg/dl Without diagnosis of diabetes mellitus "No" response to six questions in Physical Activity Readiness Questionnaire (PAR-Q), given at time of screening Exclusion Criteria: Lack of informed consent Decisionally impaired individuals Non-English speaking Acute illness within the preceding six weeks (defined as fever, new antibiotic use or unscheduled healthcare visit (for illness)) Acute alcohol intoxication Pregnancy Currently prescribed blood thinners (if undergoing muscle biopsy) Allergy to Lidocaine (if undergoing muscle biopsy) Significant peripheral neuropathies (if undergoing exercise) Significant cardiovascular impairments (if undergoing exercise)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patricia Molina, MD, PhD
Organizational Affiliation
Louisiana State University Health Sciences Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Louisiana State University Health Sciences Center
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Requests for access to biological samples or existing clinical data obtained from our subjects will be evaluated by Dr. Molina.
Citations:
PubMed Identifier
34342022
Citation
Primeaux SD, Simon L, Ferguson TF, Levitt DE, Brashear MM, Yeh A, Molina PE. Alcohol use and dysglycemia among people living with human immunodeficiency virus (HIV) in the Alcohol & Metabolic Comorbidities in PLWH: Evidence Driven Interventions (ALIVE-Ex) study. Alcohol Clin Exp Res. 2021 Sep;45(9):1735-1746. doi: 10.1111/acer.14667. Epub 2021 Aug 2.
Results Reference
derived

Learn more about this trial

Alcohol & Metabolic Comorbidities in PLWHA: Evidence Driven Interventions

We'll reach out to this number within 24 hrs