Effect of Weight Loss Diet and Pumpkin Seed Flour Consumption on Obese Women

NCT ID: NCT02086396

Last Updated: 2014-03-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

139 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-10-31

Study Completion Date

2013-09-30

Brief Summary

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This study aimed to evaluate the effect of weight loss diet combined with pumpkin seed flour consumption on diet improvement, weight loss, and glucose and cholesterol reduction in obese.

Detailed Description

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Conditions

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Obesity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Caregivers Investigators Outcome Assessors

Study Groups

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pumpkin seed flour

The pumpkin seed flour group received 20g/day of pumpkin seed flour during 12 weeks

Group Type EXPERIMENTAL

pumpkin seed flour

Intervention Type DIETARY_SUPPLEMENT

The pumpkin seed flour group received 20g/day of pumpkin seed flour during 12 weeks

Cassava flavored flour

The placebo group (cassava flour flavored) received 20g/day of cassava flour flavored during 12 weeks.

Group Type PLACEBO_COMPARATOR

Placebo (cassava flavored flour)

Intervention Type DIETARY_SUPPLEMENT

The group placebo (cassava flour flavored) received 20g/day of cassava flour flavored during 12 weeks.

Interventions

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pumpkin seed flour

The pumpkin seed flour group received 20g/day of pumpkin seed flour during 12 weeks

Intervention Type DIETARY_SUPPLEMENT

Placebo (cassava flavored flour)

The group placebo (cassava flour flavored) received 20g/day of cassava flour flavored during 12 weeks.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* age from 20 to 59 years old.
* body mass index above 30 kg/m2

Exclusion Criteria

* diabetic
* loss weight before the research
* consumption of vitamins or dietary supplement.
* pregnancy
Minimum Eligible Age

20 Years

Maximum Eligible Age

59 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Rio de Janeiro State Research Supporting Foundation (FAPERJ)

OTHER_GOV

Sponsor Role collaborator

Universidade Federal do Rio de Janeiro

OTHER

Sponsor Role lead

Responsible Party

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Anna Paula Soares de Oliveira Carvalho

Masters in Cardiovascular Sciences

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Glorimar Rosa, Doctor

Role: STUDY_DIRECTOR

Universidade Federal do Rio de Janeiro

Gláucia MM Oliveira, Doctor

Role: STUDY_CHAIR

Universidade Federal do Rio de Janeiro

Anna SO Carvalho, Master

Role: PRINCIPAL_INVESTIGATOR

Universidade Federal do Rio de Janeiro

Locations

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Federal University of Rio de Janeiro

Rio de Janeiro, Rio de Janeiro, Brazil

Site Status

Countries

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Brazil

Other Identifiers

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ACarvalho

Identifier Type: -

Identifier Source: org_study_id

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