Multiplanar Lumbopelvic Control in Patients With Low Back Pain
NCT ID: NCT02089321
Last Updated: 2014-03-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
38 participants
OBSERVATIONAL
2011-11-30
2012-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of Spinal Kinematics Between Asymptomatic Subjects and Patients With Low Back Pain
NCT02278549
Relationship Between the Sagittal Lumbopelvic Alignment and Balance Control in Adolescents With Mechanical Low Back Pain
NCT06255587
The Role of Lumbar Multifidus Characteristics in the Development of Low Back Pain
NCT03387930
Evaluation of Dynamic Stability in the Low Back Pain Patient
NCT02059317
Does the Therapist's Assessment of Movement Control in Low Back Pain Patients Correspond to an Objective Kinematic Modification
NCT05511012
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients with Low Back Pain
n= 19
Inclusion Criteria:
Between the ages of 18 and 70 years Currently seeking, but not yet initiated, treatment from a health care professional (PT, MD, DO, DC) for a chief complaint of pain between the level of the twelfth thoracic vertebrae and the coccyx Able to transition between standing, sitting, supine, prone and sidelying independently
Exclusion Criteria:
Signs of neurological impairment including diminished myotatic reflex, sensory impairment or strength deficits in a myotomal pattern No previous spine or hip surgery Serious spinal or systemic pathology Pregnancy within previous 12 months Inability to understand and follow verbal instructions in English
No interventions assigned to this group
Healthy Controls
n= 19
Inclusion Criteria:
Between the ages of 18 and 70 years No LBP episodes requiring clinical care by a health professional and/or greater than 3 days absence from work/school/recreation within the previous 5 years Able to transition between standing, sitting, supine, prone and sidelying independently
Exclusion Criteria:
No previous spine or hip surgery Serious spinal or systemic pathology Pregnancy within previous 12 months Inability to understand and follow verbal instructions in English
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age 18-70 years old
* Ability to understand and follow written and verbal instruction in English
* Seeking treatment from a physical therapist for LBP (pain below T12-L1 vertebral segment), prior to initial evaluation (no treatment provided)
Matched Controls: Control subjects will be matched for age, gender, and BMI category to patients with LBP.
* Ability to understand and follow written and verbal instruction in English
* No history of LBP during the past 5 years requiring:
* \> 3 day absence from work/school/recreation
* Clinical Care (MD, DC, DPT, MT) for LBP
Exclusion Criteria
* Pregnancy within past 12 months
* Previous spine or hip surgery
* Serious spinal or systemic pathology
* Inability to transfer from standing to supine to sidelying to prone
* Inability to stand \> 20 minutes
Matched Controls
* Pregnancy within the past 12 months
* Previous spine or hip surgery
* Inability to transfer from standing to supine to side-lying to prone
* Inability to stand \> 20 minutes
18 Years
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Regis University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Erika Nelson-Wong
Associate Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Regis University
Denver, Colorado, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NelsonWong_LBP2013
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.