Skip to content

From Blueprint to Practice: An Innovative Dynamic 9-Box Grid Improves Exercise Participation and Aerobic Capacity in Graduate Students

From Blueprint to Practice: an Innovative Dynamic 9-Box Grid for Enhancing Exercise Adherence and Aerobic Capacity in Graduate Students

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07136818
Enrollment
30
Registered
2025-08-22
Start date
2024-10-14
Completion date
2025-01-10
Last updated
2025-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Addressing Sedentary Behaviors, Bridging the Gap Between Exercise Intention and Action, Enhancing Aerobic Capacity, Improving Low Exercise Engagement

Brief summary

This study aims to develop and validate an innovative dynamic 9-square grid management model to improve aerobic capacity (AC) and physical activity participation among graduate students. The model integrates real-time exercise volume (quantified via smart wearable devices) and aerobic capacity (assessed by 12-minute run tests) into a two-dimensional grid, stratifying participants into five tiers for differentiated interventions. Using a 2 × 3 mixed-design (feedback frequency: weekly vs. monthly; time points: baseline/mid/post-intervention), 32 healthy graduate students are randomized into two groups: Weekly feedback (dynamic position updates + tailored optimization strategies). Monthly feedback (position updates at monthly intervals). Key components include: Multimodal assessment: Objective exercise metrics (Huawei Band 6), AC (12-min run), psychological scales (Exercise Identity Scale, Self-Efficacy for Exercise Scale). Tiered intervention: Customized strategies based on grid positioning (e.g., Star Talent optimization vs. Urgent Attention support). Primary outcomes: Changes in AC, total exercise volume (TEV), exercise identity, and self-efficacy. The study seeks to determine whether weekly dynamic feedback outperforms monthly feedback in sustaining behavioral change and enhancing physiological adaptation. Ethical approval was obtained from Anqing Normal University (AQNU2024110).

Interventions

BEHAVIORALDynamic 9-Square Grid Health Management with Weekly Feedback

A dual-axis management system categorizing participants into a 3x3 grid based on aerobic capacity (12-min run test) and total exercise volume (smart-device tracked). Includes weekly personalized feedback, tiered exercise prescriptions, and goal recalibration. Arm 1 receives updates every 7 days.

BEHAVIORALDynamic 9-Square Grid Health Management with Monthly Feedback

Identical grid framework as Arm 1 (aerobic capacity + exercise volume assessment), but with monthly (30-day) feedback cycles. Participants receive delayed optimization strategies and tier adjustments once per calendar month, simulating conventional health programs.

Sponsors

Hainan Normal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Graduate students aged between 18 and 30 years. * Completion of the Physical Activity Readiness Questionnaire (PAR-Q) to confirm readiness for exercise. * Completion of a sociodemographic questionnaire (including age, gender, and education level). * Confirmation of absence of exercise contraindications (e.g., conditions that may prevent safe participation in physical activity). * Confirmation of absence of cardiovascular disease. * Confirmation of absence of recent lower-limb injuries (occurring within the past 3 months or less). * Confirmation of absence of chest pain symptoms. * Ability to provide written informed consent for voluntary participation.

Exclusion criteria

* Presence of exercise contraindications identified through the PAR-Q or clinical evaluation. * History or diagnosis of cardiovascular disease (e.g., heart conditions, stroke, or related disorders). * Recent lower-limb injuries (e.g., fractures, sprains, or surgeries) within the past 3 months. * Experience of chest pain symptoms (e.g., angina or discomfort during physical exertion). * Inability to complete the required questionnaires or assessments due to cognitive or language barriers. * Presence of any uncontrolled chronic condition that could interfere with exercise participation, as determined by the researchers during screening.

Design outcomes

Primary

MeasureTime frameDescription
Change in Aerobic Capacity (12-min run distance)Baseline, Week 5 (mid-intervention), Week 9 (post-intervention).Description: Distance run in meters during standardized 12-minute field test. Measurement Tool: GPS-tracked outdoor run (Keep App + Huawei Band 6).

Secondary

MeasureTime frameDescription
Exercise Self-Efficacy (SEE-C Scale)Timeframe: Baseline and Week 9.Description: Confidence in maintaining exercise habits (0-90 scale). Measurement Tool: Chinese Self-Efficacy for Exercise Scale (Cronbach's α=0.75).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026