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Exercise Snacks and Muscular Fitness in Sedentary Young Women (ES)

2 luglio 2026 aggiornato da: Ziren Zhao, Chongqing Normal University

Effects of a 75-Minute Weekly Exercise Snack on Muscular Fitness in Sedentary Young Women

This randomized controlled study examined whether exercise snacks could improve skeletal muscle strength and related physical fitness in sedentary female university students. Eligible participants were sedentary women aged 18 to 25 years who were randomly assigned to an exercise snacks group, a regular exercise group, or a control group. The intervention lasted 8 weeks. The exercise snacks group accumulated short bouts of exercise across the day, while the regular exercise group completed more concentrated exercise sessions three times per week. The control group maintained their usual lifestyle. Muscle strength and related physical fitness were assessed before and after the intervention. The study aimed to evaluate the effectiveness, feasibility, and safety of exercise snacks in a university setting.

Panoramica dello studio

Descrizione dettagliata

Sedentary behavior is common among university students and may contribute to reduced physical fitness and lower skeletal muscle function. Exercise snacks are short bouts of physical activity performed repeatedly throughout the day and may offer a time-efficient strategy for interrupting prolonged sitting.

This single-center randomized controlled study was conducted at Chongqing Normal University. Sedentary female university students aged 18 to 25 years were screened for eligibility. Participants completed baseline assessments and were randomly allocated to an exercise snacks group, a regular exercise group, or a control group.

The intervention lasted 8 weeks. The exercise snacks group performed short exercise bouts distributed throughout the day, with a total weekly exercise volume of approximately 75 minutes. The regular exercise group performed exercise three times per week, with each session lasting approximately 25 minutes. Both intervention groups received exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion through the Tizhiyun mobile application. The control group maintained their usual study and lifestyle routines without additional study-prescribed exercise.

Primary outcomes included isokinetic muscle strength, surface electromyography, and mid-thigh isometric pull performance. Secondary outcomes included standing long jump, knee push-ups, and bodyweight squats to exhaustion. Outcome assessments were conducted at baseline and after the 8-week intervention. Adherence, perceived exertion, and exercise-related adverse events were recorded during the study period.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

90

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, Cina, 401331
        • Chongqing Normal University

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Female university students aged 18 to 25 years.
  • Daily sedentary time of at least 8 hours, assessed using a sedentary behavior questionnaire.
  • No contraindications to exercise based on the Physical Activity Readiness Questionnaire.
  • No regular exercise participation during the previous 3 months.

Exclusion Criteria:

  • Clinical conditions that make participation in exercise inappropriate.
  • Substantial body weight fluctuation during the previous 3 months.
  • Hypertension, cardiovascular or cerebrovascular disease, or use of related medications.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Exercise Snacks Group
Participants received the exercise snacks intervention for 8 weeks. Exercise was accumulated through short bouts distributed across the day, with a total weekly exercise volume of approximately 75 minutes. Participants completed approximately 11 minutes of exercise on weekdays and 10 minutes on weekends. Exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion were provided through the Tizhiyun mobile application.
Participants performed an 8-week exercise snacks program consisting of short bouts of physical activity distributed across the day. The program was performed 7 days per week, with approximately 75 minutes of exercise per week. Participants completed approximately 11 minutes of short exercise on weekdays and 10 minutes on weekends. Exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion were provided through the Tizhiyun mobile application.
Comparatore attivo: Regular Exercise Group
Participants received a regular exercise intervention for 8 weeks. Exercise was completed three times per week, with each session lasting approximately 25 minutes.
Participants performed an 8-week regular exercise program. Exercise sessions were completed three times per week on Monday, Wednesday, and Friday, with each session lasting approximately 25 minutes. Exercise guidance, reminders, adherence monitoring, and ratings of perceived exertion were provided through the Tizhiyun mobile application.
Nessun intervento: Usual Lifestyle Control Group
Participants maintained their usual study and lifestyle routines during the 8-week study period and did not receive additional study-prescribed exercise.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Isokinetic Muscle Strength
Lasso di tempo: Baseline and Week 8
Isokinetic muscle strength was assessed using an isokinetic dynamometer during standardized testing. Change from baseline to post-intervention was evaluated.
Baseline and Week 8
Surface Electromyography Activity
Lasso di tempo: Baseline and Week 8
Surface electromyographic activity was recorded during standardized muscle strength testing to evaluate neuromuscular activation.
Baseline and Week 8
Mid-Thigh Isometric Pull
Lasso di tempo: Baseline and Week 8
Maximal force generated during a standardized mid-thigh isometric pull test was assessed to evaluate whole-body isometric strength.
Baseline and Week 8

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Standing Long Jump
Lasso di tempo: Baseline and Week 8
Standing long jump distance was assessed using a standardized test of lower-body explosive performance.
Baseline and Week 8
Knee Push-Ups
Lasso di tempo: Baseline and Week 8
The number of correctly completed knee push-up repetitions was assessed using a standardized muscular endurance test.
Baseline and Week 8
Bodyweight Squats to Exhaustion
Lasso di tempo: Baseline and Week 8
The number of correctly completed bodyweight squats performed to volitional exhaustion was assessed as an indicator of lower-body muscular endurance.
Baseline and Week 8

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

20 aprile 2026

Completamento primario (Effettivo)

25 giugno 2026

Completamento dello studio (Effettivo)

25 giugno 2026

Date di iscrizione allo studio

Primo inviato

2 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

2 luglio 2026

Primo Inserito (Effettivo)

9 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

2 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • CSK2026051

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

De-identified individual participant data will not be shared outside the research team because the current informed consent and data management plans limit the use of participant data to this study and do not include external data sharing.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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