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Slow/Insufficient accrual
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Background:
Weight gain can lead to obesity and diabetes even in people living with human immunodeficiency virus (HIV). Researchers want to see if the technique intermittent calorie restriction can help overweight people with HIV as an alternative to traditional diets.
Objective:
To see if intermittent calorie restriction leads to weight loss and improved blood sugar in obese people with HIV.
Eligibility:
Adults ages 18-65 with HIV who are obese and do not have diabetes
Design:
Participants will be screened with a medical history, physical exam, and blood and urine tests.
Before starting treatment, participants will:
At the baseline visit, participants will have:
For 12 weeks, some participants will be on a standard diet. Others will restrict how much food they eat 2 days a week. On those days they will eat about 25% of their recommended calories.
Participants will keep a diary of their diet and steps.
Participants will have 4 visits during the 12-week diet and 1 visit 12 weeks after the diet ends. They will repeat previous tests.
The high prevalence of obesity coupled with chronic inflammation and immune activation places human immunodeficiency virus (HIV)-infected individuals at increased risk for metabolic complications emphasizing the need for more aggressive management of obesity and related co-morbidities in the aging HIV-infected population. The most effective treatment for obesity and metabolic syndrome is lifestyle modification, usually with a combination of caloric restriction and increased exercise. Intermittent caloric restriction (ICR) or intermittent fasting simplifies caloric restriction by severely limiting calories only a few days per week and allowing ad lib diet on the other days. Weight loss benefits are similar to those seen with conventional diets, however, data suggests possible added health benefits from intermittent fasting.
We propose to study the benefits of a 2-5 ICR strategy on weight, insulin resistance, and cardiovascular disease markers in obese HIV-infected adults with features of the metabolic syndrome. In a prospective pilot study, 50 HIVinfected adults will be randomized 1:1 to ICR or standard-of-care instruction of healthy diet and lifestyle for a 12-week intervention period. We hypothesize that ICR (2 days per week) will be an effective and acceptable diet strategy that will result in significant weight reduction, improvements in insulin sensitivity, and related metabolic parameters.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intermittent Fasting diet | Experimental | HIV positive subjects with body mass index ≥30 kg/m2 (obese) consume approximately 25% of their daily calories for 2 non-consecutive days per week, normal diet for the other 5 days, and receive healthy lifestyle counseling for 12 weeks. |
|
| Standard of Care diet | Active Comparator | HIV positive subjects with body mass index ≥30 kg/m2 (obese) receive nutritional and healthy lifestyle counseling for 12 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Intermittent fasting | Behavioral | Subject will consume approximately 25% of their daily calories for 2 days per week. The other 5 days they will eat their normal diet |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Weight | The effect of intermittent fasting was measured by change in weight between baseline and at week 12 | Assessed before 12-week intervention (baseline) and at week 12 |
| Change in Insulin Sensitivity | The effect of intermittent fasting on insulin sensitivity was measured by change in homeostatic model assessment of insulin resistance (HOMA-IR) between baseline and week 12. Homeostasis model assessment of insulin resistance (HOMA-IR) is a method to measure insulin sensitivity. Optimal insulin sensitivity is a HOMA-IR ratio less than 1. Levels above 1.9 signal early insulin resistance, while levels above 2.9 signal significant insulin resistance. | Assessed before 12-week intervention (baseline) and at week 12 |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Controlled Attenuation Parameter (CAP) Score | The effect of Intermittent fasting on body composition was evaluated using Controlled Attenuation Parameter (CAP) score from Fibroscan. Measurement of controlled attenuation parameter (CAP) is a non-invasive quantitative and qualitative assessment of liver steatosis. CAP measures ultrasonic attenuation (in dB/m) at a frequency of 3.5 MHz (on a go-and-return path). Values range from 100 to 400 dB/m. Higher levels indicate increased hepatic fat. |
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-INCLUSION CRITERIA:
Aged 18 to 65 years
HIV RNA level less than or equal to 200 copies/mL for greater than or equal to1 year (1 measure greater than or equal to 200 allowed if also <500 and preceded and followed by one or more undetectable values)
Cluster of differentiation 4 (CD4) >200 cells/mL and no active opportunistic infection or malignancy
BMI greater than or equal to 30 kg/m^2
One or more components of the metabolic syndrome as defined below.
Risk Factor: Waist circumference
Risk Factor: Triglycerides, greater than or equal to 150 mg/dL
Risk Factor: High density lipoprotein (HDL) cholesterol
Risk Factor: Blood pressure, greater than or equal to 130 / greater than or equal to 85 mmHg
Risk Factor: Fasting glucose, greater than or equal to 110 mg/dL
Fasting blood glucose >60 mg/dL at screening
Willingness to allow sample storage for future research
Able to provide informed consent
EXCLUSION CRITERIA:
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| Name | Affiliation | Role |
|---|---|---|
| Colleen M Hadigan, M.D. | National Institute of Allergy and Infectious Diseases (NIAID) | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | Maryland | 20892 | United States |
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| Label | URL |
|---|---|
| NIH Clinical Center Detailed Web Page | View source |
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Of the 35 subjects who were consented to protocol, four subjects withdrew prior to start of study, one subject was screen failure and 30 subjects started the study.
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| ID | Title | Description |
|---|---|---|
| FG000 | Intermittent Fasting Diet | HIV positive subjects with body mass index =30 kg/m2 (obese) consume approximately 25% of their daily calories for 2 non-consecutive days per week, normal diet for the other 5 days, and receive healthy lifestyle counseling for 12 weeks. |
| FG001 | Standard of Care Diet | HIV positive subjects with body mass index =30 kg/m2 (obese) receive nutritional and healthy lifestyle counseling for 12 weeks. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Intermittent Fasting Diet | HIV positive subjects with body mass index ≥30 kg/m2 (obese) consume approximately 25% of their daily calories for 2 non-consecutive days per week, normal diet for the other 5 days, and receive healthy lifestyle counseling for 12 weeks. |
| BG001 | Standard of Care Diet |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Change in Weight | The effect of intermittent fasting was measured by change in weight between baseline and at week 12 | Analysis only includes subjects who completed through Week 12 | Posted | Mean | Standard Deviation | kilograms | Assessed before 12-week intervention (baseline) and at week 12 |
|
24 weeks
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Intermittent Fasting Diet | HIV positive subjects with body mass index =30 kg/m2 (obese) consume approximately 25% of their daily calories for 2 non-consecutive days per week, normal diet for the other 5 days, and receive healthy lifestyle counseling for 12 weeks. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Localised oedema | Cardiac disorders | Systematic Assessment |
Due to the COVID 19 pandemic, study enrollment was stopped and the study did not sufficiently enroll to perform statistical comparisons as originally planned.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Hadigan, Colleen | Clinical Center | +1 301 594 5754 | hadiganc@nih.gov |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Oct 20, 2020 | Aug 30, 2022 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D000163 | Acquired Immunodeficiency Syndrome |
| D024821 | Metabolic Syndrome |
| D005215 | Fasting |
| ID | Term |
|---|---|
| D015658 | HIV Infections |
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
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| ID | Term |
|---|---|
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
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| Standard of Care | Other | Subject will receive standard of care recommendations for healthy diet and lifestyle |
|
| Assessed before 12-week intervention (baseline) and at week 12 |
| Change in Visceral Adipose Tissue | The effect of intermittent fasting was evaluated by change in visceral adiposity using total body dual energy x-ray absorptiometry (DEXA) between baseline and at week 12. | Assessed before 12-week intervention (baseline) and at week 12 |
| Change in Lipid Panel Levels | The effect of Intermittent fasting was measured by change in lipid profile levels between baseline and week 12. Lipid profile levels assessed include serum triglyceride, HDL cholesterol, LDL cholesterol, and total cholesterol levels. | Assessed before 12-week intervention (baseline) and at week 12 |
| Change in C-reactive Protein (CRP) Levels | The effect of Intermittent fasting on biomarker of inflammation was measured by C-reactive protein (CRP) levels between baseline and week 12 | Assessed before 12-week intervention (baseline) and at week 12 |
| Change in Beck Depression Inventory (BDI) Score | The effect of Intermittent fasting on mood was evaluated by change in the Beck Depression Inventory (BDI) score between baseline and week 12. The Beck Depression Inventory (BDI) is a 21-item measure of depression with each question on a 4-point scale ranging from 0=minimal to 3 = more severe (full list score values = 0,1,2,3). Total scores are a sum of individual items. Minimal depression = 0-13, mild depression = 14-19, moderate depression = 20-28, and severe depression = 29-63. The maximum score is 63 and the minimum possible score is zero. | Assessed before 12-week intervention (baseline) and at week 12 |
| Self-reported Compliance Rate With Assigned Diet | Compliance with assigned diet was assessed by participant self-reported rating. Participants used a self rating score of 0-100% with 0% = noncompliant and 100% = completely compliant with assigned diet. Compliance rate per participant was calculated using average of all daily reported scores. The overall compliance rate was averaged over all participants to get the mean compliance. | Compliance reported at Week 12 |
HIV positive subjects with body mass index ≥30 kg/m2 (obese) receive nutritional and healthy lifestyle counseling for 12 weeks. |
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Weight | Mean | Standard Deviation | kilograms |
|
|
|
| Primary | Change in Insulin Sensitivity | The effect of intermittent fasting on insulin sensitivity was measured by change in homeostatic model assessment of insulin resistance (HOMA-IR) between baseline and week 12. Homeostasis model assessment of insulin resistance (HOMA-IR) is a method to measure insulin sensitivity. Optimal insulin sensitivity is a HOMA-IR ratio less than 1. Levels above 1.9 signal early insulin resistance, while levels above 2.9 signal significant insulin resistance. | Analysis only includes subjects who completed study through Week 12 | Posted | Mean | Standard Deviation | unitless | Assessed before 12-week intervention (baseline) and at week 12 |
|
|
|
| Secondary | Change in Controlled Attenuation Parameter (CAP) Score | The effect of Intermittent fasting on body composition was evaluated using Controlled Attenuation Parameter (CAP) score from Fibroscan. Measurement of controlled attenuation parameter (CAP) is a non-invasive quantitative and qualitative assessment of liver steatosis. CAP measures ultrasonic attenuation (in dB/m) at a frequency of 3.5 MHz (on a go-and-return path). Values range from 100 to 400 dB/m. Higher levels indicate increased hepatic fat. | Analysis only includes subjects who completed study through week 12. Unable to obtain a Fibroscan on 10 participants because of body habitus. | Posted | Mean | Standard Deviation | dB/m | Assessed before 12-week intervention (baseline) and at week 12 |
|
|
|
| Secondary | Change in Visceral Adipose Tissue | The effect of intermittent fasting was evaluated by change in visceral adiposity using total body dual energy x-ray absorptiometry (DEXA) between baseline and at week 12. | Analysis only includes subjects who completed study through week 12. Ten participants were unable to complete this exam | Posted | Mean | Standard Deviation | mg | Assessed before 12-week intervention (baseline) and at week 12 |
|
|
|
| Secondary | Change in Lipid Panel Levels | The effect of Intermittent fasting was measured by change in lipid profile levels between baseline and week 12. Lipid profile levels assessed include serum triglyceride, HDL cholesterol, LDL cholesterol, and total cholesterol levels. | Analysis only includes subjects who completed study through week 12 | Posted | Mean | Standard Deviation | mg/dL | Assessed before 12-week intervention (baseline) and at week 12 |
|
|
|
| Secondary | Change in C-reactive Protein (CRP) Levels | The effect of Intermittent fasting on biomarker of inflammation was measured by C-reactive protein (CRP) levels between baseline and week 12 | Analysis only includes subjects who completed study through week 12 | Posted | Mean | Standard Deviation | mg/L | Assessed before 12-week intervention (baseline) and at week 12 |
|
|
|
| Secondary | Change in Beck Depression Inventory (BDI) Score | The effect of Intermittent fasting on mood was evaluated by change in the Beck Depression Inventory (BDI) score between baseline and week 12. The Beck Depression Inventory (BDI) is a 21-item measure of depression with each question on a 4-point scale ranging from 0=minimal to 3 = more severe (full list score values = 0,1,2,3). Total scores are a sum of individual items. Minimal depression = 0-13, mild depression = 14-19, moderate depression = 20-28, and severe depression = 29-63. The maximum score is 63 and the minimum possible score is zero. | Analysis only included subjects who completed study through week 12 and completed the questionnaire | Posted | Mean | Standard Deviation | Units on a scale | Assessed before 12-week intervention (baseline) and at week 12 |
|
|
|
| Secondary | Self-reported Compliance Rate With Assigned Diet | Compliance with assigned diet was assessed by participant self-reported rating. Participants used a self rating score of 0-100% with 0% = noncompliant and 100% = completely compliant with assigned diet. Compliance rate per participant was calculated using average of all daily reported scores. The overall compliance rate was averaged over all participants to get the mean compliance. | Analysis only included subjects who completed study through week 12. 11 subjects did not report their compliance rate. | Posted | Mean | Standard Deviation | Percentage of Compliance | Compliance reported at Week 12 |
|
|
|
| 0 |
| 14 |
| 0 |
| 14 |
| 9 |
| 14 |
| EG001 | Standard of Care Diet | HIV positive subjects with body mass index =30 kg/m2 (obese) receive nutritional and healthy lifestyle counseling for 12 weeks. | 0 | 16 | 0 | 16 | 7 | 16 |
| Diabetes mellitus | Endocrine disorders | Systematic Assessment |
|
| Impaired fasting glucose | Endocrine disorders | Systematic Assessment |
|
| Constipation | Gastrointestinal disorders | Systematic Assessment |
|
| Gastrooesophageal reflux disease | Gastrointestinal disorders | Systematic Assessment |
|
| Malaise | General disorders | Systematic Assessment |
|
| Oedema | General disorders | Systematic Assessment |
|
| Aspartate aminotransferase increased | Investigations | Systematic Assessment |
|
| Blood alkaline phosphatase decreased | Investigations | Systematic Assessment |
|
| Blood bicarbonate decreased | Investigations | Systematic Assessment |
|
| Blood cholesterol increased | Investigations | Systematic Assessment |
|
| Blood creatinine increased | Investigations | Systematic Assessment |
|
| Blood glucose increased | Investigations | Systematic Assessment |
|
| Low density lipoprotein increased | Investigations | Systematic Assessment |
|
| Abnormal weight gain | Metabolism and nutrition disorders | Systematic Assessment |
|
| Headache | Nervous system disorders | Systematic Assessment |
|
| Anxiety | Psychiatric disorders | Systematic Assessment |
|
| Micturition urgency | Renal and urinary disorders | Systematic Assessment |
|
| Chest pain | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| Upper respiratory tract infection | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
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| D015229 |
| Sexually Transmitted Diseases, Viral |
| D012749 | Sexually Transmitted Diseases |
| D016180 | Lentivirus Infections |
| D012192 | Retroviridae Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D012897 | Slow Virus Diseases |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D007333 | Insulin Resistance |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D005247 | Feeding Behavior |
| D001519 | Behavior |
| LDL Cholesterol |
|
| Total Cholesterol |
|