Resistance Exercise Effects on Fear Avoidance and Physical Function in Obese Older Adults With Low Back Pain

Resistance Exercise Effects on Fear Avoidance Beliefs and Physical Function in Obese, Older Adults With Chronic Low Back Pain

The purpose of this study is to determine if a 4 month resistance exercise program reduces the severity of low back pain, pain-related fear avoidance and improves mobility compared to standard care.

Study Overview

• Status: Completed
• Conditions: Obesity; Low Back Pain
• Intervention / Treatment: Other: normal medical care and follow up; Other: Isolated Lumbar Resistance Exercise Program; Other: Total Body Resistance Exercise Program

• Study Type: Interventional
• Enrollment (Actual): 72
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Florida
    • Gainesville, Florida, United States, 32607
      • UF&Shands Orthopaedics and Sports Medicine Institute

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 60 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• chronic low back pain for >6 months
• >3 pain episodes per week
• waist circumferences ≥102 cm for men
• waist circumferences ≥ 88 cm for women
• willing and able to participate in regular exercise for 14 weeks
• using pain medications to control low back pain
• free of abnormal cardiovascular responses during a screening graded maximal walk test

Exclusion Criteria:

• unable to walk
• participating in regular resistance exercise training (>3X week) in the past 6 months
• pain symptoms are too severe and prevent strength testing or walking
• acute back injury
• spinal stenosis that precludes walking one block due to neurogenic claudication
• back surgery within the past 2 years
• current use of weight loss interventions (drugs; exercise interventions)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Standard care; Subjects will receive normal medical care and follow up during the four month study period if assigned to this group.	Other: normal medical care and follow up; physical activity/ nutrition guidelines will be provided and reviewed with the participant as part of standard care; telephone contact will be made weekly to encourage adherence to the health guidelines
Active Comparator: Isolated Lumbar Resistance Exercise Program; Lumbar extension exercise protocol to increase strength and reduce pain.	Other: Isolated Lumbar Resistance Exercise Program; lumbar extension, two set of 10-15 repetitions, once a week for two weeks; lumbar extension, one set of 10-15 repetitions, three times a week, week 3 to 4 months
Active Comparator: Total Body Resistance Exercise Program; Training protocol for 1 set for each exercise: leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, biceps curl, calf press and abdominal curl	Other: Total Body Resistance Exercise Program; exercises: leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, biceps curl, calf press and abdominal curl, one set of 10-12 repetitions, three time per week, week one to 4 months

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
10 centimeter Visual Analog Scale (VAS); Change from Baseline at 1, 2, 3 and 4 Months	The VAS scale will range from 0-10 cm, where a rating of "0" reflects no pain, and a "10" rating represents "worst pain imaginable. Subjects will complete the VAS at the indicated time intervals to document any change in their pain levels.	Baseline, 1, 2, 3 and 4 Months
Tampa Scale of Kinesiophobia (TSK); Change from Baseline at 1, 2, 3 and 4 Months	Fear avoidance beliefs will be measured using the 11 item TSK. Subjects will complete the TSK at the indicated time intervals to document any change in their fear avoidance beliefs.	Baseline, 1, 2, 3 and 4 Months
Fear-Avoidance Beliefs Questionnaire (FABQ); Change from Baseline at 1, 2, 3 and 4 Months	The FABQ is a tool based on theories of fear and avoidance behavior and focuses specifically on beliefs about how physical activity and work affect low back pain. Subjects will complete the FABQ at the indicated time intervals to document any change in their fear and avoidance behavior.	Baselinje, 1, 2, 3 and 4 Months
Pain Catastrophizing Scale (PCS); Change from Baseline at 1, 2, 3 and 4 Months	The PCS will be used to assess the effect of the chronic back pain on rumination on pain symptoms and helplessness. Subjects will complete the PCS at the indicated time intervals to document any change in their thoughts of their pain symptoms.	Baseline, 1, 2, 3 and 4 Months
Modified Oswestry Disability Index (ODI); Change from Baseline at 1, 2, 3 and 4 Months	The ODI is responsive to intervention treatments for low back pain, is reliable, and corresponds well with several global patient disability measures. Subjects will complete the ODI at the indicated time intervals to document any change in their low back pain.	Baseline, 1, 2, 3 and 4 Months
Roland Disability Survey (RDS); Change from Baseline at 1, 2, 3 and 4 Months	The RDS assesses physical disability and mental function with low back pain; this survey is sensitive to treatment interventions, and is reproducible and consistent and correlated well with other global ratings and disability measures. Subjects will complete the RDS at the indicated time intervals to document any change in their physical disability and mental function with their low back pain.	Baseline, 1, 2, 3, and 4 Months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Graded Treadmill Exercise Test; Change from Baseline at 4 Months	Maximal aerobic fitness, or oxygen consumption (VO2max) will be determined using a walking symptom-limited graded exercise test. Subjects will complete the exercise test at the indicated time intervals to document any change in their aerobic fitness.	Baseline and 4 Months
Chair Rise Time, Stair Climb Time and Gait Assessment; Change from Baseline at 4 Months	Chair rise time will be measured as the participant moves from a sitting to a full standing position. The time to walk up one flight of stairs will be measured by having the participants walk up one flight of stairs consisting of 12 steps as quickly as possible. Gait will be assessed by having the participants walk across a 26' portable walkway. Subjects will complete these motions at the indicated time intervals to document any change.	Baseline and 4 Months
7-day Pedometer Test; Change from Baseline at 4 Months	Community ambulation will be estimated using a 7-day pedometer test in which participants will wear a StepWatch® step activity monitor. Subjects will complete this test at the indicated time intervals to document any change in their ambulation.	7 day period at Baseline and 4 Months
Ultrasound Muscle Thickness; Change from Baseline at 4 Months	The ultrasound technique that will be used to capture muscle thickness changes in the paraspinal and multifidus muscles. Subjects will be tested at the indicated time intervals to document any change.	Baseline and 4 Months
Muscle Strength; Change from Baseline at 1, 2, 3 and 4 Months	Assessments of strength (1 repetition maximum, 1-RM) will be determined for all muscle groups trained. Subjects will be assessed at the indicated time intervals to document any change.	Baseline, 1, 2, 3 and 4 Months

Collaborators and Investigators

• Sponsor: University of Florida

Study record dates

Study Major Dates

• Study Start: November 1, 2010
• Primary Completion (Actual): February 1, 2014
• Study Completion (Actual): February 1, 2014

Study Registration Dates

• First Submitted: November 5, 2010
• First Submitted That Met QC Criteria: November 29, 2010
• First Posted (Estimate): November 30, 2010

Study Record Updates

• Last Update Posted (Estimate): February 14, 2014
• Last Update Submitted That Met QC Criteria: February 12, 2014
• Last Verified: February 1, 2014

More Information

Terms related to this study

• Keywords: low back pain; obese; fear avoidance; disability and low back pain; chronic low back pain in obese older adults
• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Back Pain; Low Back Pain
• Other Study ID Numbers: 258-2010