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Effects of Training With a Pressure Cuff on Cellular Energy Activity

Influence of Short-Term Conventional Cuff-Assisted Training on Mitochondrial Capacity: A Non-Invasive Investigation

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07494721
Enrollment
51
Registered
2026-03-27
Start date
2026-07-01
Completion date
2026-12-01
Last updated
2026-04-01

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

Conditions

Physical Deconditioning

Brief summary

This study investigates low-load, cuff-assisted training to improve mitochondrial capacity. The intervention is carried out using automated pressure cuffs, applying an individualized pressure of 70% of the limb occlusion pressure. This approach reflects the current scientific consensus for safe and effective use in clinical populations. Within a rehabilitation setting, two training modalities are compared: intermittent strength training and alternating continuous endurance training. Muscle oxygen saturation is measured non-invasively using near-infrared spectroscopy.

Interventions

DIAGNOSTIC_TESTApplication of pressure cuffs during strength training

Pre/Post comparison of mitochondrial capacity of the m. vastus lateralis muscle and muscle morphology between the groups.

DIAGNOSTIC_TESTApplication of pressure cuffs during endurance training

Pre/Post comparison of mitochondrial capacity of the m. vastus lateralis muscle and muscle morphology between the groups

DIAGNOSTIC_TESTConventional clinical rehabilitation program without the use of pressure cuffs

Pre/Post comparison of mitochondrial capacity of the m. vastus lateralis muscle and muscle morphology between the groups

Sponsors

Spital Thurgau AG
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion: * Medically confirmed generalized deconditioning with reduced muscle strength * Medical certification of suitability for functional lower-extremity strength training * Written informed consent after an adequate reflection period Exclusion: * Unstable arrhythmias, myocardial ischemia, symptomatic blood pressure drops or hypertension (\>160/100 mmHg despite medication) * History of thrombosis or acute swelling/skin discoloration of the legs * Dizziness, confusion, cyanosis, or unexplained fatigue * Participant's wish to withdraw or not participate

Design outcomes

Primary

MeasureTime frame
Determination of changes in the mitochondrial capacity of skeletal muscle (of the thigh muscle, vastus lateralis; measured non-invasively)From enrollment to the end of treatment at 6 weeks.

Secondary

MeasureTime frameDescription
Minimum and maximum oxygen saturation (SmO₂) during application of pressure cuffs (measured via NIRS)From enrollment to the end of treatment at 6 weeks.
Changes in total hemoglobin (tHb) as a measure of local blood volume (measured via NIRS)From enrollment to the end of treatment at 6 weeks.
Assessment of subjective functional mobility using the "Lower Extremity Functional Scale" (LEFS) questionnaireFrom enrollment to the end of treatment at 6 weeks.Maximal Score: 80; Minimal Score: 0; Higher Score indicates better functional mobility

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026