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Ankle ProprioceptionNCT07307339

The Acute Effects of Blood Flow Restriction on Ankle Muscle Reaction Time and Proprioception in Healthy Individuals

A study testing Blood Flow Restriction in people with Ankle Proprioception and Blood Flow Restriction, run by Uludag University at 1 site in Turkey (Türkiye).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

his randomized controlled crossover study aims to investigate the acute effects of lower limb blood flow restriction (BFR) on ankle joint proprioception, postural control, and muscle activation in healthy adults. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Ankle Proprioception, Blood Flow Restriction
What is being tested?
Blood Flow Restriction
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
24 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Sep 2025to 10 Jan 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Aged between 18 and 40 years
  • No known neuromuscular or cardiovascular disease

Who cannot join

  • History or presence of cardiac, coronary artery, or peripheral arterial disease
  • Presence or history of varicose veins, hypertension, diabetes mellitus, or pulmonary disease
  • History of pulmonary embolism or deep vein thrombosis
  • Use of medications affecting the central nervous or cardiovascular systems
  • Use of oral contraceptives or anticoagulants
  • Pregnancy
Show all 9Show fewer
  • Open wounds or significant scar tissue at the cuff application site
  • History of lower extremity musculoskeletal injury or surgery
  • Any neurological, vascular, or systemic condition that may interfere with test performance

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Uludag University

    Bursa, 16059

Other trials in Turkey (Türkiye)

About this study

his randomized controlled crossover study aims to investigate the acute effects of lower limb blood flow restriction (BFR) on ankle joint proprioception, postural control, and muscle activation in healthy adults. Each participant will complete test sessions under BFR (60% individualized arterial occlusion pressure) and control (20 mmHg sham) conditions. Outcome measures include joint position sense, kinesthesia, static and dynamic balance performance, and electromyographic (EMG) activity and reaction times of selected lower limb tibialis anterior and peroneus longus muscles.

Read the detailed description

Lateral ankle sprains are among the most common musculoskeletal injuries and may lead to chronic ankle instability (CAI), partly due to impaired proprioception and neuromuscular control. Blood flow restriction (BFR) training is widely used to augment muscular adaptations with low external loads; however, its acute effects on joint proprioception and sensorimotor control, particularly at the ankle joint, remain unclear and may be detrimental under certain conditions. This randomized controlled crossover trial will examine the effects of a single-session lower limb BFR application on ankle joint position sense, kinesthesia, static and dynamic balance, and EMG-based reaction time and activity of lower limb muscles in healthy adults. Participants aged 18-40 years without recent ankle sprain, neuromuscular, cardiovascular, or thromboembolic disease will undergo standardized proprioception tests using an isokinetic dynamometer, static balance tests on a force platform, Y-balance test, and inversion simulation platform assessments under BFR (60% arterial occlusion pressure) and low-pressure control (20 mmHg) conditions. Individual arterial occlusion pressure (AOP) will be determined using Doppler ultrasound, and BFR will be applied with a pneumatic cuff at the most proximal thigh. All measurements will be performed on the dominant lower limb with sessions scheduled at the same time of day to minimize circadian variability. The primary hypothesis is that acute lower limb BFR will worsen ankle joint proprioception and sensorimotor control compared with the control condition, potentially indicating a transient increase in injury risk during BFR-assisted activities.

Being tested
Blood Flow Restriction, Sham Blood Flow Restriction
Keywords
ankle, proprioception, blood flow restriction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Blood Flow RestrictionOther

    Arm Description: Participants perform balance/proprioception tests under lower limb blood flow restriction at % 60 AOP.

  • Sham Blood Flow RestrictionOther

    Sham BFR Description: Participants perform the same tests with sham(20 mmHg) blood flow restriction

Study groups in NCT07307339
Study groupRoleWhat they receive
Blood Flow RestrictionExperimentalParticipants perform balance/proprioception tests under lower limb blood flow restriction at % 60 AOP.
Receives: Other: Blood Flow Restriction
Sham BFRSham comparatorSham BFR Description: Participants perform the same tests with sham(20 mmHg) blood flow restriction
Receives: Other: Sham Blood Flow Restriction

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Ankle Joint Position Sense Error (degrees)

    Absolute error (degrees) between target and reproduced angles during passive and active joint position sense tests in inversion and plantar flexion, measured with an isokinetic dynamometer.

    Measured: day 1 and day 2

  2. Static Balance Performance

    Center of pressure path length (mm) in single-leg and tandem stance with eyes open/closed on force platform (HUR SmartBalance).

    Measured: day 3

  3. Change in Kinesthesia Threshold (degrees)

    Minimal angular displacement (degrees) at which movement is first perceived in inversion and plantarflexion.

    Measured: day 1 and day 2

  4. Static balance performance

    sway velocity (mm/s) in single-leg and tandem stance with eyes open/closed on force platform (HUR SmartBalance).

    Measured: day 3

  5. static balance performance

    sway area (mm^2) in single-leg and tandem stance with eyes open/closed on force platform (HUR SmartBalance).

    Measured: day 3

Secondary outcomes (3)
  1. Y-Balance Test Reach Distances (cm)

    Anterior, posteromedial and posterolateral reach distances of the tested limb.

    Measured: day 4

  2. Peroneus Longus and Tibialis Anterior Reaction Time (ms)

    Time from onset of platform-induced inversion to EMG activation exceeding 2× resting activity.

    Measured: day 4

  3. Lower Limb EMG Activity (%MVIC)

    Mean EMG amplitude normalized to maximal voluntary isometric contraction values.

    Measured: day 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Dec 2025
  2. Study start1 Sep 2025
  3. Primary completion30 Dec 2025 (estimated)
  4. Study completion10 Jan 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
Arm 1: Experimental - Blood Flow Restriction Participants perform balance and proprioception tests under lower-limb blood flow restriction at 60% arterial occlusion pressure. Arm 2: Sham Comparator - Sham Blood Flow Restriction Participants perform the same balance and proprioception tests with sham blood flow restriction at 20 mmHg. This is a randomized crossover study, and all participants complete both conditions in a randomized order.
Masking
None (open label)
Enrolment
24 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07307339
Sponsor's protocol ID
2025-15/31
Status last verified
Nov 2025
First submitted
14 Nov 2025
Last updated
29 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Tugran M, Sekir U, Hasanoglu M, Gur H, Akova B. The Acute Effects of Blood Flow Restriction on Ankle Muscle Reaction Time and Proprioception in Healthy Individuals. J Sports Sci Med. 2026 Sep 1;25(3):691-700. doi: 10.52082/jssm.2026.691. eCollection 2026 Sep.

    PubMed 42713581

Questions about this trial

What is this clinical trial studying?

A study testing Blood Flow Restriction in people with Ankle Proprioception and Blood Flow Restriction, run by Uludag University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 29 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Ankle Joint Position Sense Error (degrees) (time frame: day 1 and day 2). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07307339, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Dec 2025.

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