Overweight and Obesity Clinical Trial
Official title:
Effects of Eight Weeks of Concurrent Exercise Training and Time-restricted Feeding (16/8) on Body Composition, Muscle Endurance, Metabolism, Cardiovascular Risk Factors, and Dietary Intake in Males and Females.
| NCT number | NCT03823872 |
| Other study ID # | HE18247 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | October 8, 2018 |
| Est. completion date | March 31, 2020 |
| Verified date | August 2020 |
| Source | North Dakota State University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Overweight and obesity prevalence in adolescents and adults continues to remain significantly high in the United States. While diet and exercise improve many consequences of obesity, dietary strategies are not always nutrient sufficient and manageable long-term. Thus, highly complaint dietary strategies that lead to fat loss, while maintaining muscle mass, are needed. Time-restricted feeding (TRF) may be an ideal dietary approach for reducing fat mass and cardiovascular disease risk, while diminishing the loss of muscle mass and strength associated with obesity and aging. TRF, unlike continuous energy restriction, does not require a restrictive energy intake10. TRF requires individuals to consume calories within a set window of time (example = 8 hours), inducing a fasting window of 16 hours per day. There are few human studies on TRF that measure their effects in combination with both aerobic and resistance training. One recent study found an 8-hour TRF program (16-hour fast) improved insulin sensitivity, decreased fat mass, and maintained muscle mass in resistance-trained males after 8 weeks. Thus, the feasibility of TRF as dietary approach should be investigated further.The aims of this study are to: 1) determine whether time-restricted feeding (TRF) is an effective dietary strategy for reducing fat mass while preserving fat-free mass with aerobic and resistance training; 2) evaluate potential changes in health-related biomarkers (cardiovascular profile and anabolic-catabolic hormones) and muscle health indicators (mass, strength and quality) after 8 weeks of concurrent training with TRF; and 3) examine the influence of caloric intake and macronutrient consumption on muscle health in the TRF and normal feeding (NF) groups pre- to post-concurrent resistance training.
| Status | Completed |
| Enrollment | 21 |
| Est. completion date | March 31, 2020 |
| Est. primary completion date | December 16, 2019 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 35 Years to 60 Years |
| Eligibility |
Inclusion Criteria: - Body mass index 25.0-34.9 kg/m2, generally healthy and mobile. Exclusion Criteria: - Currently smoke tobacco. - e-cigarettes, or used smokeless tobacco. - Diagnosed neuromuscular disease. - Diagnosed diabetes, - Diagnosed high blood pressure. - Diagnosed cancer. - Previous heart attack or other chronic heart related conditions. - Difficulty moving without assistive devices. - Difficulty walking one quarter mile. - Taking medications that influence muscle size. - Previous bariatric surgery. - Greater than 350 lbs in body mass. - Currently on a dietary or exercise program. - At risk for disordered eating via self-report. |
| Country | Name | City | State |
|---|---|---|---|
| United States | North Dakota State University | Fargo | North Dakota |
| Lead Sponsor | Collaborator |
|---|---|
| Kyle Hackney | University of Nebraska |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change from Baseline Body mass after 8 weeks | mass kg of subject on a calibrated scale | change from 8 weeks | |
| Primary | Change from Baseline fat mass after 8 weeks | fat mass in kg of the subject measured by DXA | change from 8 weeks | |
| Primary | Change from Baseline lean mass after 8 weeks | lean mass kg of the subject measured by DXA | change from 8 weeks | |
| Secondary | Change from Baseline insulin after 8 weeks | insulin µIU/mLvia blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline high-sensitivity C-reactive protein (Hs-CRP) after 8 weeks | Hs-CRP in mg/Lvia blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline hemoglobin A1c after 8 weeks | hemoglobin A1c % via blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline triglycerides after 8 weeks | triglycerides in mg/dL via blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline cholesterol 8 weeks | cholesterol mg/dL via blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline HDL after 8 weeks | HDL mg/dL from blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline LDL after 8 weeks | LDL mg/dL via blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline VLDL after 8 weeks | VLDL mg/dL from blood spot testing | change from 8 weeks | |
| Secondary | Change from Baseline estradiol after 8 weeks | estradiol pg/mL from saliva testing | change from 8 weeks | |
| Secondary | Change from Baseline progesterone after 8 weeks | progesterone pg/mL from saliva testing | change from 8 weeks | |
| Secondary | Change from Baseline testosterone after 8 weeks | testosterone pg/mL from saliva testing | change from 8 weeks | |
| Secondary | Change from Baseline cortisol after 8 weeks | cortisol pg/mL from saliva testing | change from 8 weeks | |
| Secondary | Change from Baseline lower body strength after 8 weeks | biodex assessment in Newtons | change from 8 weeks | |
| Secondary | Change from Baseline upper body strength after 8 weeks | handgrip assessment in kg | change from 8 weeks |
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