Strength, Pain and Function in Operation Iraqi Freedom/Operation Enduring Freedom Amputees: A Nurse-Managed Program
NCT00942890 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44
Last updated 2018-04-10
Summary
The purpose of this randomized control study is to determine if administering neuromuscular electrical stimulation (NMES) to the thigh muscles of a below the knee amputee is more effective than the current standard of care in preserving thigh muscle strength. In addition, this study will examine the NMES treatment effects on the participant's gait, quality of life, functional performance of standing, walking, and stair climbing, and symptoms associated with residual and phantom limb pain. The primary aim is to compare NMES plus standard rehabilitation (treatment group) to the standard rehabilitation (control group) by measuring lower extremity muscle strength. The secondary aims are to compare NMES treatment group to the control group by measuring Quality of Life (QOL) and the symptoms associated with residual \& phantom limb pain. In addition to the specific aims, this study will also examine the two groups for functional performance and gait patterns after prosthetic fitting.
Conditions
- Traumatic Amputation
Interventions
- DEVICE
-
NMES (EMPI 300PV stimulator) plus standard of care
In addition to the standard rehabilitation, the NMES treatment group will receive neuromuscular electrical stimulation to the quadriceps muscle of the residual and intact limb. The name of the NMES device is EMPI 300PV. NMES training will consist of performing 15 to 20 minute stimulation sessions with a 5-minute patient treatment log, 5 times per week for 12 weeks. During each training session, 15 NMES contractions per leg will be completed. Each contraction will be elicited by an electrical impulse (300PV) generated by a battery-operated device. This will be performed at home.
- BEHAVIORAL
-
TMARP standard of care
The usual care is 12 weeks of the Traditional Military Amputee Rehabilitation Program (TMARP). TMARP training starts 1week after surgical closure of the residual limb. Physical Therapy performs Pre-Prosthetic Training for about 6 weeks, preparing for the prosthetic. After pre-prosthetic training, patients are fitted with their prosthetic leg and began post-prosthetic training with PT. The training focus is lower limb prosthetic proficient in ambulation.
Sponsors & Collaborators
-
Walter Reed National Military Medical Center
collaborator FED -
United States Naval Medical Center, San Diego
collaborator FED -
University of Tennessee
lead OTHER
Principal Investigators
-
Laura A Talbot, PhD · UTHSC
-
Michelle Kane, PhD · Walter Reed National Military Medical Center
-
Michael Rosenthal, PhD · Navy Medical Center San Diego
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-04-30
- Primary Completion
- 2015-08-31
- Completion
- 2015-08-31
Countries
- United States
Study Locations
More Related Trials
-
Use of Neuromuscular Electrostimulation (NMES) for Treatment or Prevention of ICU-Associated Weakness
NCT00709124 ·Status: COMPLETED ·Phase: NA
-
TENS for Phantom Limb Pain Prevention Following Major Amputation
NCT02496351 ·Status: UNKNOWN ·Phase: NA
-
The Effect of Neuromuscular Electrical Stimulation (NMES)
NCT00765739 ·Status: COMPLETED ·Phase: PHASE2
-
A Clinical Trial of Mirror Treatment for Phantom Pain
NCT02912975 ·Status: COMPLETED ·Phase: NA
-
Electro-Neuro-Muscular Stimulation in ICU
NCT02011282 ·Status: COMPLETED ·Phase: NA
-
NMES for Rehab After Surgery
NCT04784962 ·Status: COMPLETED ·Phase: NA
-
the Influence of Virtual Reality Approach on Phantom Pain in Trans Tibial Amputation
NCT06262503 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Neuromuscular Electrical Stimulation for Intensive Care Unit-acquired Weakness Assessment
NCT02706587 ·Status: UNKNOWN ·Phase: PHASE3
-
Influence of Electrode Positioning and Current Type on Fatigue, Force and Discomfort
NCT04200677 ·Status: COMPLETED ·Phase: NA
-
Neuromuscular Electrical Stimulation in Critically Ill Patients Aged 80 and Over
NCT07127991 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Effect of Prophylactic TMR and RPNI on Neuroma and Phantom Limb Pain
NCT05344261 ·Status: WITHDRAWN ·Phase: NA
-
Electromagnetic Stimulation of the Phrenic Nerve of Intubated Patients
NCT04946110 ·Status: COMPLETED ·Phase: NA
-
Effect of All-Stim 2 Quadriceps Treatments on Limb Muscle Strength In Mechanically Ventilated Patients
NCT02332187 ·Status: TERMINATED ·Phase: NA
-
NMES and Chronic Ankle Instability
NCT04322409 ·Status: UNKNOWN ·Phase: PHASE1
-
Effect of Neuromuscular Calf Stimulation and Intermittent Pneumatic Compression on Lower Limb Venous Hemodynamics
NCT01939288 ·Status: COMPLETED ·Phase: NA
-
Functional Inspiratory Versus Expiratory Muscle Electrical Stimulation on Weaning Outcomes in Mechanically Ventilated Patients
NCT07204821 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Electrophysiological Comparison of mAP and mADM Using EMG
NCT03360825 ·Status: COMPLETED
-
Transcutaneous Electric Muscle Stimulation (TEMS) in Septic Patients
NCT01071343 ·Status: COMPLETED ·Phase: NA
-
Electrical Stimulation of the Muscle Pumps of the Leg
NCT02532556 ·Status: COMPLETED ·Phase: NA
-
Electrical Muscle Stimulation in the Development of Acquired Weakness in Patients With Severe Sepsis and Septic Shock
NCT03765489 ·Status: COMPLETED ·Phase: NA
-
Effects of Neuromuscular Electrical Stimulation Parameters on Torque, Fatigue, and Oxygen Extraction
NCT05061056 ·Status: COMPLETED ·Phase: NA
-
Pulsed Electromagnetic Therapy Versus Whole Body Vibration on Quadriceps Strength Post Burn
NCT06662552 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Electrical Stimulus Therapy for Chronic Phantom Limb Pain
NCT03030079 ·Status: COMPLETED ·Phase: NA
-
Neuromuscular Electrical Stimulation in a Patient on Invasive Mechanical Ventilation (MOVCARE)
NCT07188350 ·Status: RECRUITING ·Phase: NA
-
Effects of Neuromuscular Electrical Stimulation on Muscle Mass and Strength in Critically Ill Patients After Cardiothoracic Surgery
NCT02391103 ·Status: COMPLETED ·Phase: NA