Effects of Physical Exercise and a Nutritional Supplement on Body Composition, Metabolic Function, and Overall Health in Adults With a Metabolically Challenging Profile
Recruiting
N/AInterventional Study
AgingAdults With Overweight and ObesitySupplementationExercise
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
50 – 65
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
70 (estimated)
Sponsor
University of Valencia · Other
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Early-onset metabolic disturbances (such as mild hyperglycemia, subclinical dyslipidemia, excess body fat, and reduced functional capacity) represent one of the major public health challenges among middle-aged and older adults. Although body mass index (BMI) remains the primary clinical criterion for classifying excess weight, growing evidence indicates that BMI does not adequately discriminate ca…
Early-onset metabolic disturbances (such as mild hyperglycemia, subclinical dyslipidemia, excess body fat, and reduced functional capacity) represent one of the major public health challenges among middle-aged and older adults. Although body mass index (BMI) remains the primary clinical criterion for classifying excess weight, growing evidence indicates that BMI does not adequately discriminate cardiometabolic risk, particularly in individuals classified as overweight who present elevated body fat levels (Wu et al., 2024).
Several studies have identified altered metabolic phenotypes that do not meet the criteria for obesity, including the so-called "metabolically unhealthy normal weight" (MUNW) or "metabolically unhealthy non-obese" phenotypes. These individuals are characterized by excess body fat, central adiposity, and alterations in glucose and lipid metabolism despite having a non-obese BMI (Stefan, 2020). This profile is associated with increased insulin resistance, low-grade systemic inflammation, and elevated cardiovascular risk, underscoring the need for targeted interventions in "metabolically challenged" individuals. Xiong et al. (2024) demonstrated that metabolic health status independently predicts cardiovascular risk, even when BMI is within non-obese ranges. This evidence supports the rationale of the present project: to intervene in a group of adults without clinical obesity (BMI \< 30 kg/m²) but presenting at least two indicators of mild metabolic dysfunction.
Nutritional supplements with thermogenic properties that promote fat oxidation and satiety-such as phenylcapsaicin, an analog of capsaicin designed to improve bioavailability and reduce pungency, thereby enhancing tolerability in adults-may offer a promising complementary strategy. Recent studies have shown that low doses of phenylcapsaicin were sufficient to increase fat oxidation during exercise, reduce respiratory exchange ratio, and lower maximal heart rate during submaximal testing compared with placebo (Jiménez-Martínez et al., 2023a). Furthermore, additional research reported that phenylcapsaicin improved strength performance, reduced perceived exertion, and attenuated markers of muscle damage following resistance training (Jiménez-Martínez et al., 2023b). These findings suggest that thermogenic and fat-oxidation-enhancing supplementation may act as a safe and effective metabolic modulator, particularly when combined with exercise, positioning it as an innovative strategy for adults presenting mild metabolic risk.
The present study would integrate: (1) a multicomponent functional exercise program designed to improve strength, balance, and aerobic capacity in older adults; (2) a thermogenic and fat-oxidation-enhancing nutritional supplement as a safe metabolic activation strategy; (3) a standardized dietary control protocol to isolate the specific effects of the supplementation; (4) dual-energy X-ray absorptiometry (DXA) for precise body composition assessment; (5) hormonal and lipid biomarkers to evaluate underlying physiological mechanisms; and (6) validated questionnaires addressing quality of life, sleep, and appetite to capture the holistic dimension of this stage of adulthood.
This multidimensional approach would provide an innovative intervention for a growing yet underexplored population: non-obese but metabolically challenged adults at increasing cardiometabolic risk.
References:
* Jiménez-Martínez P, Sánchez-Valdepeñas J, Cornejo-Daza PJ, Cano-Castillo C, Asín-Izquierdo I, Alix-Fages C, Pareja-Blanco F, Colado JC. Effects of different phenylcapsaicin doses on neuromuscular activity and mechanical performance in trained male subjects: a randomized, triple-blinded, crossover, placebo-controlled trial. Front Physiol. 2023a Aug 2; 14: 1215644.
* Jiménez-Martínez P, Cornejo-Daza PJ, Sánchez-Valdepeñas J, Asín-Izquierdo I, Cano-Castillo C, Alix-Fages C, Pareja-Blanco F, Colado JC. Effects of different phenylcapsaicin doses on resistance training performance, muscle damage, protein breakdown, metabolic response, ratings of perceived exertion, and recovery: a randomized, triple-blinded, placebo-controlled, crossover trial. J Int Soc Sports Nutr. 2023b Dec; 20 (1): 2204083.
* Stefan N. Metabolically healthy and unhealthy normal weight and obesity. Endocrinol Metab (Seoul). 2020 Sep;35(3):487-493.
* Xiong Q, Zang Y, Li J, An Y, and Yu S. Comparison of cardiovascular disease risk association with metabolic unhealthy obesity identified by body fat percentage and body mass index: Results from the 1999-2020 National Health and Nutrition Examination Survey. PLoS One. 2024 Aug 14; 19 (8): e0305592.
* Wu Y, Li D, and Vermund SH. Advantages and limitations of the body mass index (BMI) to assess adult obesity. Int J Environ Res Public Health. 2024 Jun 10; 21 (6): 757.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria: Individuals will be eligible to participate in the study if they meet all of the following criteria:
1. Age: Between 50 and 65 years at the time of screening.
2. Weight status (non-obese): Body mass index (BMI) between 25.0 and 29.9 kg/m² (overweight range, without clinical obes…
Inclusion Criteria: Individuals will be eligible to participate in the study if they meet all of the following criteria:
1. Age: Between 50 and 65 years at the time of screening.
2. Weight status (non-obese): Body mass index (BMI) between 25.0 and 29.9 kg/m² (overweight range, without clinical obesity).
3. Metabolically challenged profile (non-obese): Presence of at least two of the following criteria, in addition to the specified BMI range:
A) Altered body composition (primary criterion): Body fat percentage ≥ 30% in women or ≥ 25% in men, assessed by DXA.
B) Borderline metabolic markers (one or more):
* Fasting glucose: 100-125 mg/dL
* Triglycerides: ≥ 150 mg/dL
* HDL cholesterol: \< 50 mg/dL in women or \< 40 mg/dL in men
* LDL cholesterol: ≥ 130 mg/dL
C) Sedentary lifestyle:
Low or very low physical activity level, defined as ≤ 600 MET·min/week according to the IPAQ questionnaire.
4. Clinical and functional status:
* Clinically stable condition, without acute disease or recent decompensation.
* Ability to perform moderate-intensity exercise three times per week, according to medical assessment.
5. Previous treatment and lifestyle:
* No participation in structured exercise programs (≥ 2 days/week) during the previous 6 months.
* No intensive hypocaloric diets or medical weight-loss treatments during the previous 3 months.
6. Administrative and ethical aspects:
* Ability to understand study explanations and follow instructions.
* Signed informed consent prior to initiation of any study procedures.
Exclusion Criteria: Individuals presenting any of the following conditions will be excluded from the study:
1. Clinical obesity or anthropometric extremes:
* BMI ≥ 30.0 kg/m² (obesity).
* Any weight-related or clinical condition that, in the judgment of the principal investigator, contraindicates participation.
2. Relevant or uncontrolled chronic diseases:
* Previous diagnosis of type 1 or type 2 diabetes mellitus.
* Moderate or severe cardiovascular disease (e.g., ischemic heart disease, heart failure, uncontrolled clinically significant arrhythmias).
* Moderate or severe renal, hepatic, or respiratory disease.
* Neurological or musculoskeletal disorders limiting or contraindicating the prescribed exercise program.
3. Pharmacological treatments interfering with energy metabolism or body weight:
Current use (or use within the previous 3 months) of:
* Weight-loss medications or GLP-1 receptor agonists
* Systemic corticosteroids at moderate or high doses
* Thyroid hormones at non-replacement doses
* Anabolic agents or other drugs significantly affecting body composition
4. Specific prior supplementation: Use of capsaicin, phenylcapsaicin, or other thermogenic or appetite-modulating supplements within the previous 3 months.
5. Functional or cognitive limitations:
* Cognitive, psychiatric, or mental health disorders that may impair study comprehension or protocol adherence.
* Physical limitations preventing safe participation in exercise.
6. Substance use:
* Alcohol consumption at levels considered high risk (\> 20 g/day).
* Heavy smoking (\> 10 cigarettes/day), unless deemed clinically stable by the investigator.
7. Other exclusion criteria:
* Concurrent participation in another clinical trial or interventional study.
* Any other condition that, in the judgment of the principal investigator, may pose additional risk to the participant or significantly interfere with study outcomes.
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.
