Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT07291765

Blood Flow Restriction Training in Acute Geriatric Rehabilitation

Led by University Hospital, Bonn · Updated on 2026-05-14

60

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Background: Older adults have a reduced ability to build and maintain muscle mass due to age-related changes in the muscular system. The resulting sarcopenia can lead to a number of health problems and limitations, such as an increased risk of falling and reduced mobility, which can affect quality of life and increase the risk of disease. To increase muscle mass and strength, high-intensity resistance training with loads of 70 to 85% of the repetition maximum (1RM) is recommended. However, this type of training poses a major challenge in the rehabilitation sector, as there is also an increased risk of injury due to physical limitations in old age. According to current research, low-intensity occlusion training could therefore represent a safe and effective training alternative. The aim of this study is therefore to examine the feasibility and effects of blood flow restriction training (BFR) on general health in older adults in a rehabilitative setting.

CONDITIONS

Official Title

Blood Flow Restriction Training in Acute Geriatric Rehabilitation

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults over 65 years old with a two-week hospitalization for acute rehabilitation after a fracture near the hip joint
Not Eligible

You will not qualify if you...

  • Sickle Cell Anemia
  • Changes to blood vessels at the site of tourniquet application, such as stents

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

St. Marien-Hospital Köln

Cologne, North Rhine-Westphalia, Germany, 50668

Actively Recruiting

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Research Team

A

Alexander Franz, Dr. med., B.Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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