Effects of "Weekend Warrior" Exercise on Muscle Strength and Cardiorespiratory Finess in Sedentary Female University Students

July 15, 2026 updated by: Zhao Fangyuan, Chongqing Normal University
This randomized controlled trial evaluated the effects of a weekend warrior exercise pattern on muscle strength and cardiorespiratory fitness in sedentary female university students. Forty participants were randomly assigned to either a weekend warrior group or a regular exercise group. Both groups completed 150 minutes of moderate-intensity jogging and resistance exercise per week for 8 weeks, but the weekly exercise sessions were distributed differently. Body composition, functional muscular performance, and aerobic capacity were assessed before and after the intervention.

Study Overview

Detailed Description

This was an 8-week, assessor-blinded randomized controlled trial involving 40 sedentary female university students aged 18 to 25 years. Participants were randomly assigned in a 1:1 ratio to either a weekend warrior group or a regular exercise group.

The weekend warrior group exercised on two consecutive days per week, completing 50 minutes of jogging and 25 minutes of resistance training per session. The regular exercise group exercised on three days per week, including two 50-minute jogging sessions and one 50-minute resistance-training session. Both groups completed 150 minutes of moderate-intensity exercise per week. Exercise intensity was maintained at a Borg Rating of Perceived Exertion of 13-14 and monitored using the talk test.

Assessments were conducted before and after the intervention. Body composition was evaluated using the InBody 770. Muscular performance was assessed using knee push-ups, sit-ups, and body-weight squats, while aerobic capacity was assessed using the 12-minute run test. All assessments were performed by the same trained assessor under standardized conditions.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, China, 401331
        • Chongqing Normal University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Female university students aged 18 to 25 years.
  2. An average daily sedentary time of at least 8 hours, as assessed using the Sedentary Behavior Questionnaire.
  3. Less than 75 minutes of vigorous-intensity physical activity or less than 150 minutes of moderate-intensity physical activity per week, as assessed using the International Physical Activity Questionnaire.
  4. Regular menstrual cycles without the use of hormonal contraceptives.

Exclusion Criteria:

  1. Identified as being at risk for participation in physical activity based on the Physical Activity Readiness Questionnaire.
  2. Current smoking or drug use.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Weekend Warrior Group
Participants completed an 8-week weekend warrior exercise program on two consecutive days per week. Each session consisted of 50 minutes of moderate-intensity jogging and 25 minutes of resistance training, totaling 150 minutes of exercise per week.
Participants exercised on two consecutive days per week for 8 weeks. Each session included 50 minutes of jogging and 25 minutes of resistance training. Exercise intensity was maintained at a Borg Rating of Perceived Exertion of 13-14 and monitored using the talk test. The total weekly exercise duration was 150 minutes.
Active Comparator: Regular Exercise Group
Participants completed an 8-week regular exercise program on three days per week, including two 50-minute moderate-intensity jogging sessions and one 50-minute resistance-training session, totaling 150 minutes of exercise per week.
Participants exercised on three days per week for 8 weeks, completing two 50-minute jogging sessions and one 50-minute resistance-training session. Exercise intensity was maintained at a Borg Rating of Perceived Exertion of 13-14 and monitored using the talk test. The total weekly exercise duration was 150 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee Push-up Performance
Time Frame: Baseline and immediately after the 8-week intervention
The number of correctly completed knee push-ups performed continuously until volitional fatigue was recorded. Higher values indicate better upper-body muscular performance.
Baseline and immediately after the 8-week intervention
Sit-up Performance
Time Frame: Baseline and immediately after the 8-week intervention
The number of correctly completed sit-ups performed continuously until volitional fatigue was recorded. Higher values indicate better abdominal muscular performance.
Baseline and immediately after the 8-week intervention
Body-weight Squat Performance
Time Frame: Baseline and immediately after the 8-week intervention
The number of correctly completed body-weight squats performed continuously until volitional fatigue was recorded. Higher values indicate better lower-body muscular performance.
Baseline and immediately after the 8-week intervention
12-minute Run Distance
Time Frame: Baseline and immediately after the 8-week intervention
The total distance covered during the 12-minute run test on a flat outdoor track was recorded in meters. A longer distance indicates better cardiorespiratory fitness.
Baseline and immediately after the 8-week intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Weight
Time Frame: Baseline and immediately after the 8-week intervention
Body weight was measured using the InBody 770 bioelectrical impedance analyzer and reported in kilograms.
Baseline and immediately after the 8-week intervention
Change in Body Mass Index
Time Frame: Baseline and immediately after the 8-week intervention
Body mass index was assessed using the InBody 770 and reported in kilograms per square meter.
Baseline and immediately after the 8-week intervention
Body Fat Percentage
Time Frame: Baseline and immediately after the 8-week intervention
Body fat percentage was assessed using the InBody 770 bioelectrical impedance analyzer and reported as a percentage.
Baseline and immediately after the 8-week intervention
Waist-to-hip Ratio
Time Frame: Baseline and immediately after the 8-week intervention
Waist-to-hip ratio was calculated by dividing waist circumference by hip circumference. Lower values generally indicate lower central adiposity.
Baseline and immediately after the 8-week intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 5, 2026

Primary Completion (Actual)

June 20, 2026

Study Completion (Actual)

July 10, 2026

Study Registration Dates

First Submitted

July 15, 2026

First Submitted That Met QC Criteria

July 15, 2026

First Posted (Actual)

July 20, 2026

Study Record Updates

Last Update Posted (Actual)

July 20, 2026

Last Update Submitted That Met QC Criteria

July 15, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CNU-WW-2026-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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