Strength, Pain and Function in Operation Iraqi Freedom/Operation Enduring Freedom Amputees: A Nurse-Managed Program
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Transtibial Amputation |
Device: NMES (EMPI 300PV stimulator) plus standard of care |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label |
| Official Title: | Strength, Pain and Function in OIF/OEF Amputees: A Nurse-Managed Program |
- lower extremity muscle strength and mobility [ Time Frame: Strength: 0, 3, 6-7, 9, 13 wks; Mobility 7, 13 weeks ] [ Designated as safety issue: No ]
- Quality of life and symptoms associated with residual limb and phantom pain [ Time Frame: QOL: 0, 7, 13 wks; Symptoms: 0, 3, 6-7, 9, 13 wks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 60 |
| Study Start Date: | April 2009 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | June 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Standard rehabilitation protocol
Both the control and treatment group will receive the current standard of care, the Amputee Rehabilitation Protocol (pre & post prosthetic training).
|
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 MNES 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.
Other Name: EMPI 300PV neuromuscular stimulator
|
|
Experimental: NMES w/ rehab
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.
|
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 MNES 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.
Other Name: EMPI 300PV neuromuscular stimulator
|
Detailed Description:
Traumatic amputation is one of the major injuries seen as a result of Operation Iraqi and Enduring Freedom with the majority being single trans-tibial amputations (TTA). TTA experience significant reductions in thigh muscle strength of the amputated limb during the first year after amputation. The residual limb is less active in daily functions of standing and walking, resulting in progressive atrophy of the quadriceps muscles in terms of a decrease in thigh diameter which is estimated at 25% of pre-amputation diameter. An intervention that may be useful in TTA rehabilitation (rehab) is neuromuscular electrical stimulation (NMES). The overall objectives of this study is to test two different approaches to prosthetic rehab as potential treatments for improving muscle strength, pain and functional performance of daily activities in military personnel with TTA. Our central hypothesis is that a Nurse Managed NMES Rehab Program will have greater improvements in muscle strength and pain as compared to the standard rehab protocol alone. The rationale for this study is that NMES could have an additive effect to the WRAMC standard of care program with greater improvements in muscle strength thus enhancing the performance of daily activities, Quality of Life (QOL), and decreasing disability. Such outcomes will ultimately result in decreased economic costs, accelerated rehab, and potentially increase the possibility of these warriors returning to duty. The specific aims are to test Nurse Managed NMES relative to standard rehabilitation by comparing: (1) Lower extremity muscle strength; (2) QOL; and (3) Symptoms associated with phantom pain. In addition to the above aims, specific aims for the post prosthetic phase of the intervention are to compare the two groups for (4) functional performance of daily activities. After pre-testing, participants aged 18 to 55 yrs with a traumatic TTA will be randomly assigned to either the 1) Nurse Managed NMES Rehab Program (n=30); or 2) WRAMC Amputee Protocol (n=30). Those in the NMES group will receive 12 weeks of electrical muscle stimulation 15 min/day, 5 days a week for 12 weeks. Both groups will receive the standard 12-week WRAMC rehab protocol. GEE methods will be used to build regression models for statistical analysis of the longitudinal data. The significance of this research is that Nurse Managed NMES may be very important for accelerating the rehab of amputees so they can achieve functional independence and regain lost muscle strength in preparation for return to duty.
Eligibility| Ages Eligible for Study: | 18 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Unilateral trans-tibial amputee;
- Military service member at the time of injury (Active Duty, Reserves or National Guard);
- Age ≥18 and ≤55 years; and
- Able to provide freely given informed consent.
Exclusion Criteria:
- A significant co-morbid medical condition (such as severe uncontrolled hypertension (over 160/100 mmHg) or neurological disorders such as epilepsy) where NMES strength training is contraindicated and/or participation would pose a safety threat or impair their ability to participate;
- Unable to speak and read English;
- Implanted cardiac pacemaker or defibrillator;
- Vision impairment where participant is classified as legally blind (we define legally blind both clinically and functionally. Clinically, it is central visual acuity of 20/200 or less in the better eye with corrective glasses. Functionally, the participant is not able to see the digital numbers on the NMES device with corrective glasses);
- Unwillingness to accept random assignment;
- Currently participating in another research study with an intervention that would potentially confound the outcome variables of this study (we will also instruct participants that joining a study after being enrolled in this protocol is also not allowed); and
- Conflicting co-morbidities including traumatic brain injury (score < 14 on Glascow Coma Scale), and a contralateral lower extremity injury that causes antalgic gait, pain > 5/10 consistently on the contralateral limb and/or a grade of < 4+/5 in lower extremity.
Contacts and Locations| Contact: Laura A Talbot, PhD | 704-687-8348 | ltalbot@uncc.edu |
| Contact: Sara Breckenridge-sproat, PhD | 202-782-7026 | Sara.Sproat@us.army.mil |
| United States, California | |
| Navy Medical Center | Recruiting |
| San Diego, California, United States, 92134 | |
| Contact: Michael D Rosenthal, PT, 619-532-7140 • Michael.Rosenthal2@med.navy.mil | |
| Contact: Jacqueline Moore, MPT, • (619)532-7126 • jacqueline.moore@med.navy.mil | |
| Principal Investigator: Michael D Rosenthal, PT, DSc | |
| Sub-Investigator: Jacqueline Moore, MPT | |
| United States, Maryland | |
| Walter Reed National Military Medical Center | Recruiting |
| Bethesda, Maryland, United States, 20889 | |
| Contact: Sarah Breckenridge-Sproat, PhD 202-782-7025 Sara.Sproat@us.army.mil | |
| Principal Investigator: Sarah Breckenridge-Sproat, PhD | |
| United States, North Carolina | |
| University of North Carolina, Charlotte | Recruiting |
| Charlotte, North Carolina, United States, 28223-0001 | |
| Contact: Laura A Talbot, PhD 704-687-8348 ltalbot@uncc.edu | |
| Principal Investigator: Laura A Talbot, PhD | |
| Principal Investigator: | Laura A Talbot, PhD | University of North Carolina, Charlotte |
| Principal Investigator: | Sara Breckenridge-Sproat, PhD | Walter Reed National Military Medical Center |
| Principal Investigator: | Michael Rosenthal, PhD | Navy Medical Center, San Diego |
More Information
No publications provided
| Responsible Party: | Laura Talbot, Professor, University of North Carolina, Charlotte |
| ClinicalTrials.gov Identifier: | NCT00942890 History of Changes |
| Other Study ID Numbers: | TSNRP Grant HU0001-08-1-TS10 |
| Study First Received: | July 15, 2009 |
| Last Updated: | February 29, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of North Carolina, Charlotte:
|
Case Management Amputation Muscle strength phantom limb pain |
ClinicalTrials.gov processed this record on May 22, 2013