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The effect of six weeks of resistance training with blood flow restriction on pain and function in chronic shoulder pain

The effect of six weeks of low-intensity blood flow restriction exercises on pain and performance in kayakers with chronic shoulder pain: clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230405057826N1
Enrollment
24
Registered
2023-09-03
Start date
2023-04-30
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

chronic shoulder pain. Pain in shoulder

Interventions

Intervention 1: Intervention Group 1: After coordinating and reviewing the records and evaluating and completing the questionnaire, people will be selected to implement the exercise program and then a

Sponsors

Shahid Beheshti University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 25 Years

Inclusion criteria

Inclusion criteria: Membership of rowers in rowing committee of Tehran province Having a history of chronic pain Having any kind of scapula dysknesia Men and women kayak rowers between 17 and 25 years old Having a body mass index less than 25 Not having a history of surgery in the neck, shoulder and chest area Absence of any medical contraindications for carrying out a resistance training program with blood flow restriction, based on the doctor's approval

Exclusion criteria

Exclusion criteria: excessive shoulder pain high blood pressure inability to perform pre-test and post-test open fracture

Design outcomes

Primary

MeasureTime frame
Strength. Timepoint: 2 days before the start of the intervention and 2 days after the end of the intervention. Method of measurement: Biodex Systems(for measure strength ).;Proprioception. Timepoint: 2 days before the start of the intervention and 2 days after the end of the intervention. Method of measurement: Biodex Systems(for measure Proprioception).;Range of motion. Timepoint: 2 days before the start of the intervention and 2 days after the end of the intervention. Method of measurement: mobee med (for measure Range of motion).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFariborz Hovanlo

Shahid Beheshti University

f_hovanloo@sbu.ac.ir+98 21 2990 5821

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026