Pistachio Intake, Satiety and Body Weight Control in Healthy Adult Women

Not Applicable

• Conditions: Healthy
• Interventions: Other: Pistachio

• Registration Number: NCT03526120
• Lead Sponsor: Rene' Yamashiro

Brief Summary

The main goal of the study is to confirm that, due to their rich nutritional content in protein, polyunsaturated fatty acids, vitamins and minerals of interest (calcium and magnesium), the regular consumption of the recommended amount of pistachios by adult women will elicit appropriate satiety and compensation in the daily energy intake, and improve diet quality, anthropometry and body composition.

Detailed Description

The expected endpoint is to demonstrate that the daily consumption of a snack of pistachios by healthy women, as recommended in the next National Program for Nutrition and Health (program PNNS, France), elicits adequate satiety and does not induce weight gain but rather improves diet quality, body composition and body fat mass distribution (less abdominal fat).

The study will be a 16 weeks randomized controlled open trial, single-center, including two parallel groups of 30 female participants (block randomization stratified on habitual energy intake and initial body weight according to the consort-statement checklist).

The main working hypothesis is a demonstration of the "non inferiority" of the effects of the pistachio intervention on body weight versus no snack consumption. The investigators hypothesize that there will be no significant difference in body weight change due to pistachios consumption. The two-sided 95% confidence interval on the intra-patient difference (before minus after the pistachio intervention) will be provided through the appropriate contrasts.

Study Timeline

• Study Start: 2018-02-27
• Study First Submitted: 2018-04-22
• Status Verified: 2018-05
• Study First Submitted QC: 2018-05-03
• Last Update Submitted: 2018-05-03
• Study First Posted: 2018-05-16
• Last Update Posted: 2018-05-16
• Primary Completion: 2019-08
• Study Completion: 2019-08

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

1. Healthy women;
2. Age: lower age limit 18 years, upper age limit: 50 years (included);
3. Body Mass Index: lower limit 19 kg/m²; upper limit 29.9 kg/m²; weight stable within ± 2 kg in the last 3 months;
4. Habitual energy intake, as indicated by an initial intake report (diary method, three days) within the 95% confidence interval (CI) of the habitual energy intake of a similar population (as provided by internal reference data collected by CREABio-RA from previous studies in similar conditions);
5. Participant not pregnant, not presently breast feeding or having breastfed in the last 3 months, and not planning to become pregnant during the study (negative pregnancy test at inclusion or morning of V1);
6. Pre-menopausal participant on effective contraception since at least 3 months (regular 28-day cycle) and who agree to continue their contraception throughout the study;
7. Participant registered with the French Social Security;
8. participant having signed informed consent

Exclusion Criteria

1. Subject under legal protection or deprived of liberty by judicial or administrative decision.
2. Currently diagnosed somatic pathology;
3. On medication affecting metabolism, weight, energy intake, or energy expenditure in the last 6 months;
4. Major psychiatric disorder, particularly eating disorders as defined by the DSM-V;
5. High level of "Restrained Eating" or "Disinhibition", as revealed by the TFEQ or similar questionnaire;
6. Strong initial dislike of nuts, specially pistachios, as revealed by questioning about food habits initial dietary questionnaire;
7. Habitual consumption of pistachios as revealed by the 3-d intake report (more than twice a week);
8. Participants smoking more than 10 cigarettes per day or planning to stop smoking in the next 3 months;
9. Currently pregnant, lactating (as specified in article L1121-5 of the Public Health Code) or less than 6 month post-partum;
10. Any kind of food allergy, especially allergies or intolerance to nuts;
11. Participant not capable of understanding the constraints of the study, who does not agree to abide, and/or unable to communicate normally with investigators;
12. Person currently participating in another clinical study, or having used up her annual entitlement to compensation for participation in biomedical studies (4500 €).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Pistachio diet	Pistachio	Incorporates 44 g (1 serving) of pistachios into a daily diet

Primary Outcome Measures

Name	Time	Method
Body weight	12 weeks	Body weight in kg

Secondary Outcome Measures

Name	Time	Method
Body fat mass	12 weeks	Body fat mass in kg
Total daily energy intake	12 weeks	Total daily energy intake in kcal
Appetite ratings	12 weeks	Appetite ratings measured on visual analogic scalls of 100 mm
Body weight index	12 weeks	Body weight index in kg/m2

Trial Locations

Locations (1)

CreaBio Rhône-Alpes; 🇫🇷 Givors, Rhône, France