Postoperative Management for Degenerative Spinal Conditions

Completed · Not applicable

Conditions studied: Spinal Degenerative Disorder

In brief

The overall objective of this study is to conduct a two-group randomized control trial (RCT) to compare which of two treatments provided by telephone - a cognitive-behavioral based physical therapy (CBPT) program focusing on self-management strategies or an education program about postoperative recovery - are more effective for improving patient-centered outcomes in older adults recovering from lumbar spine surgery for degenerative conditions. Our central hypothesis is that the CBPT intervention focusing on self-management will decrease pain and disability and improve general health, physical activity and physical function in community-dwelling adults undergoing spine surgery, through reductions in fear of movement and increases in pain self-efficacy.

Key facts

Study ID

NCT02184143

Run by

Vanderbilt University Medical Center

People needed

248

Starts

2014-08-01

Expected to finish

2018-01-01

Last updated by the study team

2019-08-02

Who can join

Age: 21 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Radiographic evidence of lumbar spinal stenosis secondary to degenerative changes
• Surgical treatment of a lumbar degenerative condition (spinal stenosis, spondylosis with or without myelopathy, and degenerative spondylolisthesis) using laminectomy with or without arthrodesis procedures
• English speaking due to feasibility of employing study personnel to deliver and assess the study intervention
• Age older than 21 years (younger individuals do not typically have a lumbar degenerative condition).

You may not qualify if…

• Patients having microsurgical techniques as the primary procedure, such as an isolated laminotomy or microdiscectomy (individuals having these minimally invasive surgical techniques tend to have a less severe case of lumbar degeneration and a shorter recovery time than individuals having arthrodesis or laminectomy without arthrodesis)
• Patients having surgery for spinal deformity as the primary indication (patients with spinal deformity as the primary spinal disorder tend to have a different recovery trajectory compared to the inclusion population)
• Patients having surgery secondary to pseudarthrosis, trauma, infection, or tumor
• Presence of back and/or lower extremity pain < 3 months indicating no history of chronic pain
• History of neurological disorder or disease, resulting in moderate to severe movement dysfunction. Including but not limited to Parkinson's disease, Multiple Sclerosis, Epilepsy, Brain tumors, Huntington's disease, Alzheimer's disease, Muscular Dystrophy, Stroke, Autonomic Nervous System disorders, Traumatic Brain Injury, Cerebral Palsy, and Amyotrophic Lateral Sclerosis
• Presence of schizophrenia or other psychotic disorder, including but not limited to Brief Psychotic disorder and Delusional disorder
• Patients not able to return to clinic for standard follow-up visits with surgeon due to time and travel limitation
• Patients having surgery under a workman's compensation claim
• Unable to provide a stable address and access to a telephone indicating the inability to participate in either the telephone-based CBPT or education program.

Where it is running

• Johns Hopkins School of Medicine — Baltimore, Maryland, United States
• Vanderbilt University Medical Center — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.