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Psychological Impacts of Exercise Snacks Versus Traditional Exercise: A Comparative Study (ES)

18 juni 2026 bijgewerkt door: Linjun Liu, Lincoln University College

This study investigates the comparative psychological impacts of a high-frequency "Exercise Snacks" (ESG) protocol versus a traditional continuous exercise (TEG) regimen on healthy young adults. Utilizing a randomized controlled trial design over a 4-week longitudinal period, 180 participants were allocated into two groups of 90, with a standby recruitment protocol employed to ensure sample size stability.

The intervention was standardized to equate total weekly exercise volume at 90 minutes. The TEG cohort performed 30-minute continuous cycling sessions three times per week, whereas the ESG cohort executed 15-minute distributed cycling sessions six times per week. To ensure physiological homogeneity and precision in workload prescription, individual baseline maximal aerobic capacity was assessed via incremental cardiopulmonary exercise testing. Based on these individual thresholds, exercise intensity for both cohorts was rigorously maintained at 40% of their respective maximal aerobic capacity throughout the intervention.

Psychometric outcomes were evaluated within 24 hours of the intervention's conclusion, focusing on three dimensions: Perceived Stress, Decision Fatigue and Cognitive Load, and Physical Activity Enjoyment. By applying Lazarus and Folkman's Transactional Model of Stress and Coping, Sweller's Cognitive Load Theory, and Self-Determination Theory, this research examines how fragmented exercise protocols interact with daily workflow and self-regulatory resources. The findings provide critical insights into the real-world viability, behavioral resistance, and psychological divergence associated with high-frequency, fragmented exercise routines compared to conventional models.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

199

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Hubei
      • Wuhan, Hubei, China, 430074
        • Wuhan Technical University

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion Criteria:

  1. Healthy young adults (aged 18-30).
  2. Body composition within the healthy range (12%-25% for males; 18%-33% for females).
  3. Able and willing to provide informed consent and adhere to the 4-week exercise protocol.

Exclusion Criteria:

  1. Pre-existing cardiovascular, metabolic, or chronic respiratory conditions.
  2. History of musculoskeletal injuries that prevent safe participation in cycling.
  3. Current engagement in regular, structured exercise exceeding 60 minutes per week.
  4. Use of medications or substances known to significantly influence heart rate, cognitive performance, or stress responses.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Fundamentele wetenschap
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Exercise Snacks Group (ESG)
Participants in this group perform high-frequency, fragmented exercise sessions. The protocol consists of six 15-minute cycling sessions per week, totaling 90 minutes of moderate-intensity activity. The exercise intensity is strictly regulated at 40% of the individual's maximal aerobic capacity, monitored via electronically braked cycle ergometers.
Participants perform high-frequency, fragmented exercise consisting of six 15-minute cycling sessions per week, totaling 90 minutes of weekly activity. The exercise intensity is strictly prescribed and maintained at 40% of the individual's maximal aerobic capacity, as determined by preliminary cardiopulmonary testing. All sessions are conducted on digitized, electronically braked stationary ergometers to ensure precise, real-time monitoring of power output and strict adherence to the prescribed workload.
Actieve vergelijker: Traditional Exercise Group (TEG)
Participants in this group follow a structured, continuous exercise protocol. The intervention involves three 30-minute sessions of continuous cycling per week, totaling 90 minutes of moderate-intensity activity. Consistent with the ESG cohort, exercise intensity is maintained at 40% of the individual's maximal aerobic capacity to ensure physiological equivalence between groups.
Participants perform structured, continuous exercise consisting of three 30-minute cycling sessions per week, totaling 90 minutes of weekly activity. To ensure physiological equivalence, the exercise intensity is also strictly maintained at 40% of the individual's maximal aerobic capacity. Participants utilize the same digitized, electronically braked stationary ergometers as the ESG group to ensure consistent monitoring of exercise duration and intensity throughout the 4-week intervention period.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Decision Fatigue and Cognitive Load (DFCL)
Tijdsspanne: Within 24 hours post-intervention.
This outcome assesses the depletion of self-regulatory resources and the cognitive strain resulting from executive function demands. It utilizes a validated psychometric instrument to evaluate task-switching costs and perceived mental exertion following daily activities.
Within 24 hours post-intervention.
Perceived Stress (PS)
Tijdsspanne: Within 24 hours post-intervention.
This outcome measures the subjective psychological distress experienced by participants. It evaluates the extent to which participants perceive situations in their lives as uncontrollable, unpredictable, and overloaded, as assessed by the standardized Perceived Stress Scale (PSS).
Within 24 hours post-intervention.
Physical Activity Enjoyment (PAE)
Tijdsspanne: Within 24 hours post-intervention.
This outcome evaluates the participant's affective response to the assigned exercise modality. It captures factors such as acute enjoyment, perceived satisfaction, and the psychological impact of logistical friction associated with the specific exercise protocol (ESG vs. TEG).
Within 24 hours post-intervention.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

16 maart 2026

Primaire voltooiing (Werkelijk)

16 juni 2026

Studie voltooiing (Werkelijk)

16 juni 2026

Studieregistratiedata

Eerst ingediend

18 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

18 juni 2026

Eerst geplaatst (Werkelijk)

24 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

24 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

18 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

There is no plan to share individual participant data to protect the privacy of the participants and ensure data security.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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