Neuromodulation for Prevention of Intensive Care Unit Acquired Weakness and Post Intensive Care Syndrome
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Muscle Atrophy
- Sponsor
- Bijan Najafi, PhD
- Enrollment
- 25
- Locations
- 1
- Primary Endpoint
- Gastrocnemius Muscle Endurance at Endpoint
- Status
- Active, not recruiting
- Last Updated
- last year
Overview
Brief Summary
Post-intensive care syndrome (PICS) encompasses persistent physical, cognitive, and psychiatric symptoms following ICU discharge, commonly triggered by serious conditions such as respiratory failure, sepsis, and mechanical ventilation. PICS prevalence is reported to be as high as 84% up to 12 months in patients with at least 2 days spent in the ICU or with mechanical ventilatory support. As a consequence, many patients do not return to they former level of function for weeks, months and even years.
Muscular affection manifested by muscle weakness is particularly seen and is provoked by a combination of damage to the nerves or directly the muscles fibers. This affection is referred to as CU-Acquired Weakness (ICUAW). One third of the time, lower extremities are affected, often due to prolonged immobilization or sedation. Evidence suggests that early mobilization reduces the incidence of ICUAW at discharge and improves the number of patients able of stand. However achieving this early intervention is not always feasible due to time or personnel constraints.
The purpose of the study is to examine the effectiveness of lower extremity neuromodulation for prevention of muscle deconditioning in patients admitted to the ICU.
Detailed Description
The purpose of the study is to examine feasibility and acceptability of lower extremity neuromodulation in patients at risk of ICUAW. This is a proof Randomized controlled trial (RCT) study for prevention. Eligible participants will be recruited from Baylor St Luke's Medical Center (Houston, Texas). Participants will be randomized to intervention group (IG) or control group (CG). The entire cohort will receive daily neuromodulation in the lower extremity (Gastrocnemius muscle, Achilles tendon) up to 1 hour. The therapy will be provided with a neuromodulation device (Tennant Biomodulator PRO®, AVAZZIA, Inc.) that works on high voltage alternative pulsed current. The device will be functional for the IG and non-functional for the CG.
Investigators
Bijan Najafi, PhD
Professor of Surgery
Baylor College of Medicine
Eligibility Criteria
Inclusion Criteria
- •Any patient older than 18 years old admitted to the ICU within 2 days.
- •Patient can be intubated with ventilatory assistance or not.
Exclusion Criteria
- •Less than 48 hours of ICU stay.
- •Major foot problems such as active lower extremity wounds, major foot deformity (e.g., Charcot Foot), and/or previous major amputations.
- •Demand-type cardiac pacemaker, implanted defibrillator, or other implanted electronic devices.
- •Any conditions that may interfere with outcomes or increase the risk of the use neuromodulation therapy based on the judgement of clinicians.
Outcomes
Primary Outcomes
Gastrocnemius Muscle Endurance at Endpoint
Time Frame: Up to 4 weeks
Gastrocnemius muscle endurance was assessed by measuring sustained involuntary muscle contractions using surface electromyography (sEMG; Delsys Trigno). During a 60-minute electrical stimulation therapy session, sEMG signals were recorded from the last two minutes of the therapy to evaluate muscle activity in response to electrical stimulation. The recorded sEMG data were normalized to the average sEMG signals captured during the same interval, yielding values in normalized units (n.u.), higher values indicate higher muscle endurance. The endpoint was defined as either the last day in the hospital or the completion of week 4 of the intervention, whichever occurred first.
Secondary Outcomes
- Ankle Strength at 4 Weeks(up to 4 weeks)
- Change in Gastrocnemius Muscle Thickness at 4 Weeks Compared to Baseline(Up to 4 weeks)
- Percentage of Tissue Oxygen Saturation at Endpoint(up to 4 weeks)
- Sural Nerve Conduction at 4 Weeks(up to 4 weeks.)
- Sural Nerve Amplitude at 4 Weeks(up to 4 weeks.)