Chronic Low Back Pain Clinical Trial
Official title:
Correlation of Trust and Outcomes Following Physical Therapy for Chronic Low Back Pain
To investigate whether changes in trust between physical therapist and patient correlate to outcomes after receiving physical therapy care. We will be utilizing established questionnaires from the medical literature and one new generated questionnaire.
1. The clinic site staff and physical therapist will fill out facility consent form to
participate as a treatment site. The treating physical therapist participant will
complete an informed consent form at their clinic site, if willing to participate via
phone call with PI. If they consent, they will fill in a demographics form and be given
an ID# that will be used for data collection by PI after informed consent received. This
will take about 5 minutes.
2. Front office staff at each physical therapy clinic will provide recruitment letter for
each new patient that potentially meets inclusion/exclusion criteria (coming into the
clinic with low back that has persisted for greater than 3 month). If patient agrees to
participate, they will fill out informed consent and HIPPA form on-line via PsychData
link provided to them by clinic staff.
3. After completing the informed consent process, the patient participant will complete the
necessary forms provided in PsychData link prior to the initial visit (Baseline
demographics, General Trust in Physician Scale, Wake Forest Scale, Trust in Physician
Scale, Patient Care Assessment Survey, Modified Oswestry Disability Index, Numeric Pain
Rating Scale) Completing the forms will take place in the waiting room as they fill out
their other normal initial paperwork needed for clinic site. This should take about
10-15 minutes. The forms will be handled electronically as the information is placed in
the PI's individual PsychData account. The therapist participants will be blinded to
research questionnaires information through the whole research project.
4. The patient then will receive a normal physical therapy initial evaluation and treatment
as directed by the physical therapist based on the patient presentation.
5. At the conclusion of the initial visit, the patient participant will complete the
necessary forms on-line through a second PsychData link (Wake Forest Scale, Trust in
Physician Scale, Patient Care Assessment Survey, Working Alliance Inventory - Short
Revised). This should take about 5-10 minutes.
6. Participant will continue to receive normal physical therapy care as directed by the
physical therapist based on patient presentation. The majority of the visits (80%) have
to be with the initial physical therapist involved in the care of the patient for that
patient participant to be eligible for the study. The patient participant will still be
eligible for all the gift cards even if they are eventually excluded due to not seeing
the same therapist for 80% of the visits.
7. At the conclusion of care for the current episode (or at the end of 6 months of
continual care by the provider), the patient participant will fill out forms on line to
a third PsychData link (Wake Forest Scale, Trust in Physician Scale, Patient Care
Assessment Survey, Working Alliance Inventory - Short Revised, Modified Oswestry
Disability Index, Numeric Pain Rating Scale, Global Rate of Change). This should take
about 10-15 minutes. If the patient is a no show and does not return for follow up
visits, the principle investigator will send follow up letters to try to get final
surveys completed.
8. After the second visit, the treating physical therapist will complete a PT Survey of
Patient Connection and Engagement form on the patient via an on-line PyschData link.
This will take less than 5 minutes. Treating therapist participant will be notified by
PI that patient has consented into the study. This on-line PsychData information will be
kept confidential from the patient participant.
9. At the conclusion of care (or 6 month time period), the physical therapist and clinic
site will complete appropriate forms (PT Survey of Patient Connection and Engagement,
number of visits, compliance (no show/cancellations), discharge disposition, and Current
Procedural Terminology (CPT) billing codes for patients care) and send back to the
principle investigator.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03243084 -
Transcranial Alternating Current Stimulation in Back Pain- Pilot Sudy
|
N/A | |
Suspended |
NCT04735185 -
Stem Cells vs. Steroids for Discogenic Back Pain
|
N/A | |
Completed |
NCT03162952 -
RAND Center of Excellence for the Study of Appropriateness of Care in CAM
|
||
Completed |
NCT03240146 -
Pulsed Shortwave Therapy Treatment for Chronic Musculoskeletal Low Back Pain
|
N/A | |
Completed |
NCT05282589 -
Lumbopelvic Manipulation Effects on Fatigue in Chronic Low Back Pain Patients
|
N/A | |
Completed |
NCT03637998 -
Physical Activity on Neurophysiologic Gene Expression Profiles of Chronic Low Back Pain
|
N/A | |
Recruiting |
NCT02289170 -
Clinical Study to Evaluate the Safety and Efficacy of Heating and Cooling Combination Therapeutic Device(OCH-S100)
|
N/A | |
Active, not recruiting |
NCT01944163 -
The IMPACT of a Referral Model for Axial Spondyloarthritis in Young Patients With Chronic Low Back Pain
|
N/A | |
Completed |
NCT02231554 -
Feldenkrais vs Back School for Treating Chronic Low Back Pain: a Randomized Controlled Trial
|
N/A | |
Recruiting |
NCT02063503 -
Identification of Prognostic Indicators for Rehabilitation in Chronic Nonspecific Low Back Pain Patients
|
N/A | |
Terminated |
NCT01620775 -
MR(Magnetic Resonance) Imaging of Neurotransmitters in Chronic Pain
|
N/A | |
Completed |
NCT01704677 -
Lumbar Disc Prosthesis Versus Multidisciplinary Rehabilitation; 8-year Follow-up
|
N/A | |
Completed |
NCT01177254 -
Exposure to Potential Cytochrome P450 Pharmacokinetic Drug-Drug Interactions Among Osteoarthritis Patients: Incremental Risk of Multiple Prescriptions
|
N/A | |
Completed |
NCT01177280 -
Prevalence of Potential Cytochrome P450 Pharmacokinetic Incident Drug-Drug Interactions Among Chronic Low Back Pain Patients Taking Opioid Analgesics and Associated Economic Outcomes
|
N/A | |
Completed |
NCT01177241 -
Cytochrome P450 Pharmacokinetic DDIs Among Patients With Chronic Low Back Pain Taking Opioids
|
N/A | |
Completed |
NCT01490905 -
A Double Blind Placebo Study to Determine the Effectiveness of Theramine on the Management of Chronic Back Pain
|
Phase 4 | |
Completed |
NCT00984815 -
Safety Study of HZT-501 in Patients Who Require Long-Term Daily Non-steroidal Anti-inflammatory Drug Treatment
|
Phase 3 | |
Completed |
NCT00761150 -
Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate to Severe Chronic Low Back Pain (CLBP)
|
Phase 3 | |
Completed |
NCT00767806 -
A Study for Patient With Chronic Low Back Pain
|
Phase 3 | |
Completed |
NCT00763321 -
Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate to Severe Chronic Low Back Pain (CLBP)
|
Phase 3 |