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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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01250262
Enrollment
72
Registered
2010-11-30
Start date
2010-11-30
Completion date
2014-02-28
Last updated
2014-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain, Obesity

Keywords

low back pain, obese, fear avoidance, disability and low back pain, chronic low back pain in obese older adults

Brief summary

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.

Interventions

OTHERnormal 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

OTHERIsolated 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

OTHERTotal 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

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Roland Disability Survey (RDS); Change from Baseline at 1, 2, 3 and 4 MonthsBaseline, 1, 2, 3, and 4 MonthsThe 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.
10 centimeter Visual Analog Scale (VAS); Change from Baseline at 1, 2, 3 and 4 MonthsBaseline, 1, 2, 3 and 4 MonthsThe 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.
Tampa Scale of Kinesiophobia (TSK); Change from Baseline at 1, 2, 3 and 4 MonthsBaseline, 1, 2, 3 and 4 MonthsFear 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.
Fear-Avoidance Beliefs Questionnaire (FABQ); Change from Baseline at 1, 2, 3 and 4 MonthsBaselinje, 1, 2, 3 and 4 MonthsThe 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.
Pain Catastrophizing Scale (PCS); Change from Baseline at 1, 2, 3 and 4 MonthsBaseline, 1, 2, 3 and 4 MonthsThe 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.
Modified Oswestry Disability Index (ODI); Change from Baseline at 1, 2, 3 and 4 MonthsBaseline, 1, 2, 3 and 4 MonthsThe 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.

Secondary

MeasureTime frameDescription
Chair Rise Time, Stair Climb Time and Gait Assessment; Change from Baseline at 4 MonthsBaseline and 4 MonthsChair 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.
7-day Pedometer Test; Change from Baseline at 4 Months7 day period at Baseline and 4 MonthsCommunity 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.
Ultrasound Muscle Thickness; Change from Baseline at 4 MonthsBaseline and 4 MonthsThe 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.
Muscle Strength; Change from Baseline at 1, 2, 3 and 4 MonthsBaseline, 1, 2, 3 and 4 MonthsAssessments 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.
Graded Treadmill Exercise Test; Change from Baseline at 4 MonthsBaseline and 4 MonthsMaximal 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026