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Completed

NCT Number: NCT04751240

Effect of Interval and Resistance Exercise on Physiological and Psychological Parameters.

The purpose of this study is to examine the physiological and psychological effects of a sprint interval and resistance training intervention on females.

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Key information

Conditions

Age range

25 year–55 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

School of Kinesiology

Auburn, Alabama, 36830, United States

About this study

Females aged 20-65 will attend 10 weeks of exercise training consisting of sprint interval training and resistance training for 30 sessions. We will examine changes in body composition, blood panel (fasting glucose, cholesterol, triglycerides), strength (bench press and back squat), aerobic capacity and psychological parameters (hardiness, affect, enjoyment, perception and self-regulation). The effects will be measured acutely after the program and 6-months after the cessation of the program.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • This population consists of: females, aged 25-55, who are: sedentary (not reporting a regular schedule of exercise over the last 3 months), and able to start an exercise program (assessed by the PARQ+)

Exclusion criteria

  • Females who are below age 25 or over age 55, who are currently exercising and have existing conditions that would exclude them from exercise.

Treatment and study plan

SIT and resistance training

Behavioral

Participants complete 30 sessions of sprints and resistance training. Outcomes are assessed acutely and at 6 months.

Primary outcomes

  1. Fat mass post

    Time frame: Change in fat mass at 13 weeks

    Changes in Fat mass in Kg assessed by idexa

  2. Fat mass retention

    Time frame: Change in fat mass at 6 months

    Changes in Fat mass in Kg assessed by idexa

  3. Lean mass post

    Time frame: Change in lean mass at 13 weeks

    Changes in Lean mass in Kg assessed by idexa

  4. Lean mass retention

    Time frame: Change in lean mass at 6 months

    Changes in Lean mass in Kg assessed by idexa

  5. Visceral Fat post

    Time frame: Change in visceral fat at 13 weeks

    Changes in Visceral Fat in Kg assessed by idexa

  6. Visceral Fat retention

    Time frame: Change in visceral fat at 13 weeks

    Changes in Visceral Fat in Kg assessed by idexa

  7. Participate perception of the program post

    Time frame: 13 weeks

    Interviews to assess participants perception of the program

  8. Participate perception of the program retention

    Time frame: 6 months

    Interviews to assess participants perception of the program

Secondary outcomes

  1. Strength - bench press

    Time frame: Change in bench press at 13 weeks

    Changes in bench press measured in Kg

  2. Strength - back squat

    Time frame: Change in back squat at 13 weeks

    Changes in back squat measured in Kg

  3. Blood glucose post

    Time frame: Changes in fasting blood glucose at 13 weeks

    Changes in fasting blood glucose

  4. Blood glucose retention

    Time frame: Changes in fasting blood glucose at 6 months

    Changes in fasting blood glucose

  5. Cholesterol post

    Time frame: Changes in Cholesterol at 13 weeks

    Changes in Cholesterol

  6. Cholesterol retention

    Time frame: Changes in Cholesterol at 6 months

    Changes in Cholesterol

  7. Triglycerides post

    Time frame: Changes in Triglycerides at13 weeks

    Changes in Triglycerides

  8. Triglycerides retention

    Time frame: Changes in Triglycerides at 6 months

    Changes in Triglycerides

Sponsors and collaborators

Lead sponsor

Auburn University

Other

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Feb 12, 2021
Registry last updated
Feb 12, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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