Homeopathy for Overweight and Obesity in Mexican Adolescents

Overweight and Obesity Clinical Trial

Official title:

Efficacy of a Multidisciplinary Intervention and Homeopahy for Overweight or Obesity in Mexican Adolescents: a Study Protocol for a Randomized Double-blind, Placebo-controlled Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03945396
• Other study ID #: HJM 0572/19-1
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: May 6, 2019
• Est. completion date: December 30, 2022

Study information

• Verified date: August 2021
• Source: Hospital Juarez de Mexico
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study evaluates the efficacy of a multidisciplinary intervention (diet, exercise, motivational support and homeopathy or placebo) for overweight and obesity in Mexican adolescents. Half of study participants will receive the multidisciplinary intervention plus Calcarea carbonica ostrearum, a homeopathic medicine, while the other half will receive the same multidisciplinary intervention plus placebo.

Description:

Overweight and obesity in children and adolescents are a major public health issue in Mexico. Whilst many factors (genetic, cultural, socioeconomic and environmental) contribute to develop obesity during childhood, a multidisciplinary intervention (nutritional, behavioral and exercise) is the best approach to improve weight loss. In Mexico, the use of homeopathy for obesity is widespread. Although there are some homeopathic medicines used for obese individuals, there is a lack of well-designed clinical trials to demonstrate its efficacy in weight loss. Calcarea carbonica ostrearum is a homeopathic mineral medicine. Previously, it has been demonstrated that Calcarea carbonica has an effect in reducing the percentage of fat in adolescents.

Therefore, a randomized, placebo-controlled, double-blind, parallel, superiority trial with a 3 month study duration, will be conducted to prove the efficacy and safety of Calcarea carbonica ostrearum in reducing weight, body mass index (BMI) and fat percentage, as well as, to prove its effect on the lipid profile, fasting serum glucose, glycosylated hemoglobin and insulin.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 60
• Est. completion date: December 30, 2022
• Est. primary completion date: November 30, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 12 Years to 19 Years

Eligibility

Inclusion Criteria:

• 12 to 19 years old.

• At least elementary school.

• Overweight (BMI = 85th but <95th percentile based on the Centers for Disease Control and Prevention growth chart) or obese (BMI =95th percentile).

• Fasting serum glucose <126 mg/dl.

• Glycosylated hemoglobin <6.5%.

• With symptoms that match with Calcarea carbonica ostrearum.

• Willingness to participate, and verbal and written consent.

Exclusion Criteria:

• Pregnancy or breastfeeding.

• Cases already undergoing treatment (homeopathic, nutritional or structured physical activity) for obesity within last three months.

• Currently use of metformin, orlistat, insulin, other antidiabetic medication, contraceptive pills, medications with effects on lipid metabolism [thiazide and loop diuretics, ß and a receptor blockers, antiepileptic drugs (carbamazepine, phenytoin, valproic acid, phenobarbital), antipsychotics (clozapine), protease inhibitors (amprenavir, indinavir, nelfinavir, ritonavir, saquinavir), tamoxifen, raloxifene, isotretinoin, acitretin, ciclosporin, azathioprine, sirolimus].

• Any condition that prevents physical exercise.

• Diabetes, hypertension, thyroid diseases, Down syndrome, mental retardation.

Related Conditions & MeSH terms

• Obesity
• Overweight
• Overweight and Obesity

Intervention

Drug:
• Homeopathic Medication
A homeopathic mineral medicine, form of impure calcium carbonate, CaCO3, which can be found in nature in different niches, from limestone to eggshells.

Other:
• Multidisciplinary intervention (Exercise program, diet, motivational support)
Exercise program: includes a five-times per week routine: warm-up during 10 to 15 minutes, then 40 minutes of aerobic exercise that will be increased progressively until reaching 60 minutes. Thereafter, muscular strength initiating 5%, and increasing until 10 to 15% of body weight. Then, 10 to 15 minutes of stretching. Finally, 5 min cool-down. Diet: Subjects will receive a balance diet calculated based on energetic needs according FAO: 15-20% of proteins, 50-60% of carbohydrate, 20-25% of fat per day. Motivational support: 50 min session where empathy and neutral understanding of the perspective and feelings of the adolescent, and his family, are fostered to motivate the change and to state realistic goals in reducing weight.

Drug:
• Homeopathic placebo
A 30 ml bottle of 30% alcohol-distilled water.

Locations

Country	Name	City	State
Mexico	Hospital Juárez de México	Mexico City

Sponsors (1)

Lead Sponsor	Collaborator
Hospital Juarez de Mexico

Country where clinical trial is conducted

Mexico, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change from baseline in mean total fasting serum glucose (mg/dL)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using an automated chemical analyzer (Advia®1200). Glucose will be assayed by the glucose-oxidase method.	At baseline and week 12.
Other	Change from baseline in mean total fasting serum triglycerides (mg/dL)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using an automated chemical analyzer (Advia®1200).	At baseline and week 12.
Other	Change from baseline in mean total cholesterol (mg/dL)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using an automated chemical analyzer (Advia®1200).	At baseline and week 12.
Other	Change from baseline in mean total high-density cholesterol (mg/dL)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using an automated chemical analyzer (Advia®1200).	At baseline and week 12.
Other	Change from baseline in mean total low-density cholesterol (mg/dL)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using an automated chemical analyzer (Advia®1200).	At baseline and week 12.
Other	Change from baseline in percentage of glycosylated hemoglobin	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using an automated chemical analyzer (Advia®1200).	At baseline and week 12.
Other	Change from baseline in mean total insulin (mU/ml)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using a chemiluminescence technique (Immulite®2000TSH Third Generation).	At baseline and week 12.
Other	Change from baseline in mean total thyroid-stimulating hormone (mU/L)	Blood samples will be collected by venipuncture in the antecubital region of patients after 10-12 hours of overnight fasting and centrifuged within 30-45 min of collection, using a chemiluminescence technique (Immulite®2000TSH Third Generation).	At baseline and week 12.
Other	Change from baseline in mean total HOMA-IR.	The homeostasis model assessment (HOMA), an epidemiologic method for assessing insulin resistance [HOMA-IR=insulin (mU/ml) X glucose (mg/dl)/405] will be used as surrogate measure of insulin sensitivity	At baseline and week 12.
Other	Change from baseline in mean total score of CES-D-R	CESDR scale measure symptoms of depression in nine different groups as defined by the American Psychiatric Association Diagnostic and Statistical Manual, fifth edition. The Total CESD-R Score is calculated as a sum of responses to all 20 questions. The range of possible scores is between 0 (for those who say 'not at all or less than one day to all 20 questions' and 60 (for those who say '5-7 days' or 'nearly every day for 2 weeks' for all 20 questions). No clinical significance: a total CESD-R score less than 16 across all 20 questions.	At baseline and week 12.
Other	Change from baseline in mean total score of Screen for Child Anxiety Related Emotional Disorders (SCARED).	Appropriate screening tool to aid the diagnosis of anxiety disorders in adolescents attending an outpatient clinic.It consists of 41 items that are rated from 0 to 2, being 0 never, 1 sometimes and 2 always. The cut-off point is 25, that is, there is a probability of at least 70% that the child or adolescent has an anxiety disorder.	At baseline and week 12.
Primary	Change from baseline in mean total weight in kilograms (kg)	Weight measured with the participants barefooted and lightly dressed, with a Tanita scale Fitscan BC-545 F segmental body composition monitor. The scale has an eight electrode body composition monitor that displays twenty readings; ten whole body and ten segmental (arms, legs and trunk area).	At baseline and week 4, 8 and 12.
Primary	Change from baseline in percentage of body fat	Body fat measured with Tanita scale Fitscan BC-545 F segmental body composition monitor. Values greater than 30% for females, and 25% for males, are considered high and of risk	At baseline and week 4, 8 and 12.
Secondary	Change from baseline in mean total body mass index (BMI).	Weight/height2 (kg/m2). Overweight (BMI = 85th but <95th percentile based on the Centers for Disease Control and Prevention growth chart) or obese (BMI =95th percentile).	At baseline and week 4, 8 and 12.
Secondary	Change from baseline in mean total fat mass index	Calculated by dividing fat weight in kilograms by height in meters squared.	At baseline and week 4, 8 and 12.
Secondary	Change from baseline in mean total lean body mass (kg).	Calculated by subtracting body fat weight from total body weight: total body weight is lean plus fat	At baseline and week 4, 8 and 12.
Secondary	Change from baseline waist-hip ratio.	Calculated as waist measurement divided by hip measurement.	At baseline and week 4, 8 and 12.
Secondary	Change from baseline in mean total lean muscle mass (kg).	Calculated by total weight of the body minus all the weight due to the fat mass.	At baseline and week 4, 8 and 12.
Secondary	Number and severity of all adverse events	Adverse event will be defined as any untoward medical occurrence in a subject without regard to the possibility of a causal relationship.	After participants consent and enrolled in the study and 15 days after study completion.