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The effect of additional BFR training on hand strength and hand function in rehabilitation patients with injuries of the upper extremity distal of the elbow

The effect of additional BFR training on hand strength and hand function in rehabilitation patients with injuries of the upper extremity distal of the elbow

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036856
Enrollment
48
Registered
2025-06-03
Start date
2025-11-24
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Injuries to the upper extremity distal to the elbow S52.50

Interventions

Group 1: The intervention group conducts BFR training with a cuff pressure of 60-70% of the arterial occlusion pressure in addition to the standard rehab program several times per week, at least ten

Sponsors

BG Klinikum Duisburg gGmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inpatient rehabilitation due to an injury to the upper extremity distal to the elbow

Exclusion criteria

Exclusion criteria: Cadiovascular deseases: - Coronary artery desease - Existing or increased risk of venous thromboembolism - Increased risk of hemorhagic stroke - Increased risk of exercise-induced rhabdomolysis - Increased risk of atrial fibrilation or heart failure - Previous use of medication that is known to increase the risk of blood clotting - Induration/Marfan syndrome - Vascular endothelial dysfunction - Previous hemophilia - Cardiopulmonary diseases - Silent myocardial ischemia - Left ventricular dysfunction - Iatrogenic changes in the arterial/venous vessels of the lower extremities - Inserted stents, bypasses - sickle cell anemia Other exclusion criteria: - Lack of knowledge of German - Bilateral injury to the upper extremities - Open wounds or infections of the extremities to be trained - Amputations on the upper extremities - Refusal to participate in the study - Lack of German language skills

Design outcomes

Primary

MeasureTime frame
The primary endpoint of the study is the improvement of pain free grip strength over the time of rehabilitation.

Secondary

MeasureTime frame
Secondary endpoints are questionnaires to seize everyday function of the upper extremity (PRWE-G), quality of life (PROMIS 29) and pain (NRS scale).

Countries

Germany

Contacts

Public ContactChristian Schmitz

BG Klinikum Duisburg gGmbH

rkos@bg-klinikum-duisburg.de+49203 7688 3110

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026