An interventional study of BFR technique in Pain Intensity, sponsored by Istanbul University - Cerrahpasa. Recruiting at 2 sites in Turkey. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-04-30.
Sponsored by Istanbul University - Cerrahpasa · Not applicable, Interventional, and Treatment
Among 54 studies in Pain by Istanbul University - Cerrahpasa — 13 open to participants now, 14 under way, none of them phase 3. Pain · Istanbul University - Cerrahpasa.
Among the 54 studies in Pain by Istanbul University - Cerrahpasa, this one is the 51st largest by planned enrollment of the 51 interventional ones that give a count, is one of 11 that started in 2024, is one of 50 with no phase, reaches primary completion later than 2 of the 13 other live ones, and was the 29th registered.
10,060 studies on the registry are indexed under Pain; 1,651 are open to participants now.
Browse Pain studies →13 of the 54 studies in Pain by Istanbul University - Cerrahpasa are open now, in 1 country. Recruiting first, the newest first:
Istanbul University - Cerrahpasa · Sites in Turkey
Ages 18–65 · Women only
Istanbul University - Cerrahpasa · Sites in Turkey
Ages up to 30 min · Healthy volunteers
Istanbul University - Cerrahpasa · Sites in Turkey
Ages 18–65
Istanbul University - Cerrahpasa · Sites in Turkey
Ages 35–65
Istanbul University - Cerrahpasa · Sites in Turkey
Ages 4–6
By country, each count listing its studies:
Of the 929 Pain studies recruiting now, 384 (41%) set no upper age limit and 434 (47%) stop at 75 or younger; 146 take children under 18; 222 take healthy volunteers.
This study: 18 Years to 35 Years · all sexes · healthy volunteers too.
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54 studies; the count open now beside each. This study's row is marked.
First in 2016; this study’s year is marked. 11 started in 2024.
This study's planned enrollment of 15 is below the median of 66 across 8,497 interventional studies indexed under Pain.
Median enrollment 80 across the 51 interventional studies, 32 across the 3 observational. Of the 39 that completed or were terminated, 1 (3%) have results posted.
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Istanbul University - Cerrahpasa is the lead sponsor of 701 studies on the registry; 211 are open to participants now.
3 of the studies in Pain by Istanbul University - Cerrahpasa that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT07860983Istanbul University - CerrahpasaPhysical and Psychosocial Outcomes of 16-Week Classroom-Based Morning Exercise Program | 2027-03-01 |
| NCT07319858Istanbul University - CerrahpasaThe Effect of Using Multifunctional Baby Carrier With Heart Surgery | 2027-08 |
| NCT07324343Istanbul University - CerrahpasaWhich Patient Group Shows Greater Improvement With Patient Education Alone in Rotator Cuff-Related Shoulder Pain? - A Cohort Study | 2027-09-01 |
Add all 3 to your calendar (.ics) → With an account.
Among the 54 studies in Pain by Istanbul University - Cerrahpasa, from their registry updates:
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The aim of our study is to determine and evaluate the effects of blood flow restriction technique on pain, biomechanical properties and strength of the muscle in delayed onset muscle pain in healthy individuals. A Double Blind, Randomized Controlled, prospective study was planned.
All participants will be taken into the DOMS creation protocol. Participants will then be divided into 80% intensity BFR and 20% intensity Blood Flow Restriction technique (BFR) groups and will be included in an exercise protocol accompanied by BFR application.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
%80 intensity BFR technique will be applied to this group.
Other: BFR technique
%20 intensity BFR technique will be applied to this group.
Other: BFR technique
For BFR application, Airbands brand, wireless, automatic training cuffs will be used. During application, it will be ensured that the device module faces forward and the cuff will be fixed in the correct position by wrapping the band around the metal ring. There will be a space between the skin and the cuff that can fit two fingers. The cuff will then be paired via Bluetooth with the Airbands app installed on the phone. BFR cuffs will be placed proximal to the biceps brachii muscle and pressure will be applied. The cuff will be inflated to automatically detect limb pressure. BFR application with 80% pressure to one group of participants and 20% pressure to the other group will be applied simultaneously with the exercise.
Visual analog scale
it will be used for assessment of pain intensity, It is scored between 0-10, and higher scores indicate that the situation is getting worse.
Time frame: 2 months
myoton
it will be used for assessment of muscle tonus and biomechanic properties, scores are changin according to different parameters.
Time frame: 2 months
dynamometer
it will be used for assessment of myscle strength, lower scores indicate that the situation is getting worse.
Time frame: 2 months
dolorimeter
it will be used for assessment of pain thresold pressure, lower scores indicate that the situation is getting worse.
Time frame: 2 months
Plan to share: No
No publications or documents are linked to this record.
Started Apr 2024 (actual). Primary completion is estimated for May 2024, 1 month after the start.
Of 3,734 non-industry interventional studies with no phase under Pain, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 23. This study's planned 1 month is below that.
Counting every sponsor, half of 3,833 studies reached it within 10 months; a quarter within 4 and three quarters within 23.
How these figures are worked out, and which studies are left out of them.
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