Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

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

15 juli 2026 uppdaterad av: 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.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Faktisk)

40

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, Kina, 401331
        • Chongqing Normal University

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen

Tar emot friska volontärer

Ja

Beskrivning

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.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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.
Aktiv komparator: 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.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Knee Push-up Performance
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Body Weight
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

5 mars 2026

Primärt slutförande (Faktisk)

20 juni 2026

Avslutad studie (Faktisk)

10 juli 2026

Studieregistreringsdatum

Först inskickad

15 juli 2026

Först inskickad som uppfyllde QC-kriterierna

15 juli 2026

Första postat (Faktisk)

20 juli 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

20 juli 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

15 juli 2026

Senast verifierad

1 juli 2026

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • CNU-WW-2026-01

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

OBESLUTSAM

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera