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Research on the effect of walking combined with blood flow restriction exercise on the physical function of sedentary college students

Research on the effect of walking combined with blood flow restriction exercise on the physical function of sedentary college students

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097728
Enrollment
Unknown
Registered
2025-02-25
Start date
2024-10-08
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

None

Interventions

walk training with blood flow restriction (trial1):0%, 40%, 60%, 80% BFR combined with 5-minute walking exercise
walking training (trial1):0%, 80%, 60%, 40% BFR combined with 5-minute walking exercise
walking training (trial2):walking training
walking training with blood flow restriction (trial2):walking training with blood flow restriction
control group (trial2):no additional interventions

Sponsors

Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1) Assessed by the Chinese version of the short volume of the International Physical Activity Scale (IPAQ) [20] : the physical activity value is not more than 1500 MET-min/week, the sitting time is more than 6 hours/day (including 6 hours), and the exercise frequency is not more than 3 times /week, and the exercise time is not more than 30 minutes; 2) No contraindications to exercise testing, such as severe cardiovascular diseases, respiratory diseases, musculoskeletal diseases, and metabolic diseases, were assessed by the Physical Activity Readiness Questionnaire (PAR-Q) [21]; 3) Informed consent.

Exclusion criteria

Exclusion criteria: 1) Exercise regularity (more than 3 times a week of moderate intensity exercise, each time lasting at least 20min); 2) There are cognitive disorders, movement disorders, major diseases; 3) Poor compliance.

Design outcomes

Primary

MeasureTime frame
Blood presure(trial1);6-minute walk test (trial2);

Secondary

MeasureTime frame
SpO2(trial1);Heart rate(trial1);RPE(trial1);RPD(trial1);MAP(trial1);30-second sit-to-stand-to-sit test (trial2);timed up-and-go test (trial2);handgrip strength (trial2);sleep quality (trial2);anxiety (trial2);depression (trial2);

Countries

China

Contacts

Public ContactHuagang Hu

Soochow University

huhuagang@suda.edu.cn+86 139 1310 3099

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 15, 2026