Exercise Intervention for Unilateral Amputees With Low Back Pain
Low Back Pain
About this trial
This is an interventional treatment trial for Low Back Pain
Eligibility Criteria
Inclusion Criteria:
- Between 18-60 years of age
- English speaking
- Suffering from chronic LBP (>3 months with ≥3 pain episodes per week)
- Baseline pain of ≥3 points out of 10 on the NRSPain scale
- Amputation ≥1 year prior and their current prosthesis must have been worn for at least 6 months (prosthesis K-Level of K2 or greater, indicating the subject is able to ambulate and traverse low-level environmental barriers such as curbs, stairs, or uneven surfaces).
- Must have regular access to a computer for skype, or a mobile phone or iPAD to perform facetime
Exclusion Criteria:
- Acute back injury
- Any other chronic back pathology (i.e. herniated disc, ankylosing spondylosis, other related neurologic disease)
- Pain symptoms or functional limitations (including those that may require assistive devices) that preclude participation in resistance exercise or physical activity
- Back surgery within the past two years that restrict daily physical activities
- Currently enrolled in any other resistance or strengthening exercise interventions
- Pregnant
Sites / Locations
- University of Florida
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Home-Based Resistance Exercise Intervention Group
Wait-List Control Condition Group
Participants in the HBRX group will be coached through six phases of the intervention with two weeks per phase. Exercise will use body weight and resistance exercise bands. A set of commercial elastic resistive bands and a stability pad (TheraBand, Inc.) will be provided to each participant to keep for personal use after their participation in the study. The use of elastic bands for resistance training can induce similar results in neuromuscular adaptations as well as strength to those achieved by weight machines and free-weights.
Participants who are assigned to the CON group will wait to participate in the resistance training after a three month wait period. Participants will follow all instructions provided to them by their physician and care team, but will be asked to refrain from starting any new strengthening exercise protocols or begin any new physical therapies during this time. The participants will be contacted by phone on a monthly basis during the study period to determine if any changes in LBP symptoms have occurred. At month three, these participants will also receive the elastic resistive bands and a stability pad.