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Effect of Different Frequencies Weekly Training in Overweight/Obese Women

Primary Purpose

Sensitivity Training Groups

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Resistance training
Sponsored by
Francesco Campa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Sensitivity Training Groups

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

overweight or obese

Exclusion Criteria:

-

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    High weekly training frequency

    Low weekly training frequency

    Arm Description

    three sessions a week of resistance training

    one workouts per week

    Outcomes

    Primary Outcome Measures

    Fat mass
    anthropometric measurements

    Secondary Outcome Measures

    Handgrip strength
    mechanical dynamometer

    Full Information

    First Posted
    January 12, 2018
    Last Updated
    January 18, 2018
    Sponsor
    Francesco Campa
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03410329
    Brief Title
    Effect of Different Frequencies Weekly Training in Overweight/Obese Women
    Official Title
    Comparison of the Effect of Different Frequencies Weekly Training on Body Composition, Cardiometabolic Risk Factors and Handgrip Strength in Overweight and Obese Women
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    December 1, 2016 (Actual)
    Primary Completion Date
    June 1, 2017 (Actual)
    Study Completion Date
    June 27, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Francesco Campa

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The aim of this study was to evaluate the effects of a resistance training programme of one or three times a week on body composition, cardiometabolic risk factors and handgrip strength in overweight and obese women
    Detailed Description
    This study aimed to determine the effects of supervised structured 6 months resistance training and a restricted caloric diet on body composition, cardiometabolic risk factors and handgrip strength in overweight and obese women. 45 women were randomly assigned to one of two groups: a group with a high-weekly frequency of three times a week (HIGH) and a group that performed only one weekly session (LOW).HbA1c, percentage of fat mass and handgrip strength were taken before and after the intervention period.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Sensitivity Training Groups

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    45 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    High weekly training frequency
    Arm Type
    Experimental
    Arm Description
    three sessions a week of resistance training
    Arm Title
    Low weekly training frequency
    Arm Type
    Experimental
    Arm Description
    one workouts per week
    Intervention Type
    Other
    Intervention Name(s)
    Resistance training
    Intervention Description
    Physical activity
    Primary Outcome Measure Information:
    Title
    Fat mass
    Description
    anthropometric measurements
    Time Frame
    24 weeks
    Secondary Outcome Measure Information:
    Title
    Handgrip strength
    Description
    mechanical dynamometer
    Time Frame
    24 weeks
    Other Pre-specified Outcome Measures:
    Title
    HbA1c
    Description
    It was measured by exchange high-performance liquid chromatograph using standardised laboratory procedures
    Time Frame
    24 weeks

    10. Eligibility

    Sex
    Female
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: overweight or obese Exclusion Criteria: -

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    Effect of Different Frequencies Weekly Training in Overweight/Obese Women

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