Low Back Pain, Recurrent Clinical Trial
— CLBPOfficial title:
Treatment of Veterans With Chronic Low Back Pain
Verified date | July 2018 |
Source | VA Office of Research and Development |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to assess the effectiveness of hypnosis in the treatment of chronic low back pain.
Status | Completed |
Enrollment | 161 |
Est. completion date | June 30, 2018 |
Est. primary completion date | February 15, 2010 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Chronic low back pain for at least 6 months - Pain severity at least 5 on a 0-10 scale - Pain is primarily musculoskeletal/mechanical - Adults, at least 18 years of age Exclusion Criteria: - Acute and cancer pain - Neuropathic etiology - Severe psychopathology - Active substance abuse - Significant cognitive deficit - Previous participant of the pilot study on hypnosis chronic low back pain |
Country | Name | City | State |
---|---|---|---|
United States | Michael E. DeBakey VA Medical Center, Houston, TX | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change From Pre-Treatment to 1-week Post Treatment on Brief Pain Inventory-Pain Intensity Scale | The change score measures the difference between Pre-Treatment Brief Pain Inventory Pain Intensity Scale scores (Numerical Rating Scale (NRS): 0 no pain - 10 worst pain) and the 1-week Post--Treatment Brief Pain Inventory-Pain Intensity Scale scores for 4 items. Change is calculated as pre-treatment minus post treatment. | Subjects change on this scale from Pre-Treatment to 1 week post treatment | |
Secondary | Change From Pre-treatment to 1- Week Post Treatment on Brief Pain Inventory-Interference Scale | The change score measures the difference between pre-treatment scores on the Brief Pain Inventory-Interference Scale (NRS: 0 no interference - 10 complete interference) and 1- week post treatment scores for the 10 items. Change is calculated as pre-treatment minus post treatment. | Subjects change on this scale from Pre-Treatment to 1-week post treatment | |
Secondary | Change From Pre Treatment to 1-week Post Treatment on Pittsburgh Sleep Quality Index (PSQI) | The change score is the difference between pre-treatment scores on the Pittsburgh Sleep Quality Index (PSQI) and the 1-week post-treatment scores. Positive values indicate a reduction in sleep problems. The PSQI was scored on 19 items with 7 component scores ranging from 0 no difficulty falling asleep to 3 severe difficulty, then component scores added to create global score ranging from 0 no difficulty falling asleep to 21 severe difficulty falling asleep. | Subjects change on this scale from Pre-treatment to 1-week post treatment |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03852667 -
The Effect of Secondary Prevention in Patients With Recurrent Low Back Pain
|
N/A | |
Completed |
NCT02235207 -
Effectiveness of Fustra—Exercise Program in Neck and Low Back Pain
|
N/A | |
Terminated |
NCT00973024 -
A Dose-ranging Study of the Safety and Effectiveness of JNJ-42160443 as add-on Treatment in Patients With Low Back Pain
|
Phase 2 | |
Active, not recruiting |
NCT00908102 -
Managing Non-acute Low Back Symptoms in Occupational Health: Two Trials
|
N/A | |
Completed |
NCT04979403 -
Efficacy of Two Physiotherapy's Approaches in Chronic Low Back Pain: Is Addressing Psychosocial Factors Beneficial?
|
N/A | |
Completed |
NCT05223946 -
Treatment and Companion Diagnostics of Lower Back Pain Using SCENAR and Passive Medical Radiometry (MWR)
|
N/A | |
Recruiting |
NCT03680287 -
Effects of Sleep Disruption on Drug Response
|
Phase 2 | |
Not yet recruiting |
NCT04542798 -
CRF vs WCRF or PRF-DRG in CLBP of FJ Origin and RFA Failure of MBDR: Central Sensitization and Aberrant Nerve Sprouting
|
N/A | |
Recruiting |
NCT05840302 -
Effectiveness of a Pain Neuroscience Education Programme on Physical Activity in Patients With Chronic Low Back Pain
|
N/A | |
Completed |
NCT06143319 -
Structural White and Gray Matter Correlates of Impaired Muscle Control and Deficient Pain Processing
|
||
Completed |
NCT03328689 -
Back2LiveWell: Community Based Prevention of Back Pain Flare-ups
|
N/A | |
Recruiting |
NCT05350254 -
Implementation of the MAINTAIN Instrument for Patients With Dysfunctional Spinal Pain
|
N/A | |
Completed |
NCT04592094 -
Evaluation of Performances and Safety of the Medical Device Blueback® Physio for Patients With Chronic Low Back Pain
|
N/A | |
Completed |
NCT04436003 -
GDS Muscle and Articulation Chain Treatment for Chronic LBP and Spinal Stenosis
|
N/A | |
Completed |
NCT04943640 -
The Additional Effect of Different Taping Applications in Patients With Lumbar Radiculopathy
|
N/A | |
Completed |
NCT05682287 -
The Effect of Radiofrequency of 448 kHz on Pain and Function
|
N/A | |
Recruiting |
NCT04074798 -
Hyperventilation in Patients With Chronic Low Back Pain
|
N/A | |
Recruiting |
NCT03984864 -
Preference, Exercise Therapy Adherence and Efficacy Low Back Pain
|
N/A | |
Recruiting |
NCT05706103 -
Exercise Therapy for Recurrent Low Back Pain: Unraveling the Puzzle of Peripheral Muscle and Central Brain Changes
|
N/A | |
Active, not recruiting |
NCT03427099 -
The Effect of a Developed Perioperative Rehabilitation Pathway Following Lumbar Arthrodesis
|
N/A |