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Auto-regulated Blood Flow Restriction in Athletes With Recurrent Ankle Sprain

P

Prince Sattam Bin Abdulaziz University

Status

Completed

Conditions

Ankle Sprain
Ankle Instability

Treatments

Other: Auto-regulated Blood Flow Restriction Training
Other: Non-regulated Blood Flow Restriction Training
Other: Control group

Study type

Interventional

Funder types

Other

Identifiers

NCT06962943
REC-23-08-28-02-PG
University of Sharjah (Other Identifier)

Details and patient eligibility

About

Ankle injuries, especially lateral ankle sprains, are prevalent in physically active individuals. Blood Flow Restriction Training (BFRT) has emerged as a promising method, employing partial arterial occlusion and full venous occlusion with low resistance to induce metabolic stress and achieve outcomes akin to heavy resistance training. This Randomized Controlled study explores the application of BFRT in addressing Chronic Ankle Instability (CAI), focusing on its efficacy in strength gains of extrinsic foot muscles, and potential benefits in functional performance.

Full description

Ankle injuries, especially lateral ankle sprains, are prevalent in physically active individuals. Blood Flow Restriction Training (BFRT) has emerged as a promising method, employing partial arterial occlusion and full venous occlusion with low resistance to induce metabolic stress and achieve outcomes akin to heavy resistance training.

This Randomized Controlled study explores the application of BFRT in addressing Chronic Ankle Instability (CAI), focusing on its efficacy in strength gains of extrinsic foot muscles, and potential benefits in functional performance.

At the Sharjah University Medical Campus, 45 athletes from Shabab Al Ahli Club, aged 18-40, participated in this randomized control study. We randomly allocated the participants into three equal groups, with 15 individuals in each group. We recruited the first group to an auto-regulated blood flow restriction training plus traditional treatment program (ARBFRT+TT), the second group to a non-regulated blood flow restriction training plus traditional treatment program (NRBFRT+TT), and the third group to a traditional treatment program only without BFRT (TT group). We assessed extrinsic foot muscle strength using an isokinetic device and functional performance using Functional Ankle Disability Index (FADI) and Rate of perceived exertion scale (RPES), both pre- and post 6-week treatment.

Enrollment

45 patients

Sex

Male

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age ranges from 18 to 40 years.
  • No other health related conditions such as diabetes or hypertension.
  • Unilateral or bilateral CIA.
  • Male Athletes.

Exclusion criteria

  • Knee or hip injury within the last 3 months.
  • Previous ankle surgery.
  • Any contraindication for BFRT application such as venous insufficiency, arterial insufficiency, history of DVT.
  • Spinal lesion affecting lower limb function.
  • Females

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

45 participants in 3 patient groups, including a placebo group

Auto-regulated blood flow restriction training (ARBFRT+TT)
Experimental group
Description:
This group was recruited to conduct auto-regulated blood flow restriction exercise for 30-min, three times a week for six weeks by a trained physiotherapist.
Treatment:
Other: Auto-regulated Blood Flow Restriction Training
Non-regulated blood flow restriction training (NRBFRT+TT)
Active Comparator group
Description:
This group was recruited to conduct non-regulated blood flow restriction exercise for 30-min, three times a week for six weeks by a trained physiotherapist.
Treatment:
Other: Non-regulated Blood Flow Restriction Training
Control group
Placebo Comparator group
Description:
The control group was recruited to conduct no blood flow restriction exercise (Cuff with 0 pressure) 30-min, three times a week for 6 weeks.
Treatment:
Other: Control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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