Preliminary Validation of the Integral of Pain Relief as a Measure of Pain Relief in Chronic Pain Patients
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Chronic Pain
- Sponsor
- Wilderman Medical Clinic
- Enrollment
- 97
- Locations
- 1
- Primary Endpoint
- Patient's Global Impression of Change (PGIC)
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The purpose of this study is to provide evidence for the empirical and clinical utility of a novel pain relief measure, the IPR, dimensions of which will be validated against the present gold standards for pain measurement.
Detailed Description
There are a number of validated unidimensional and multidimensional tools used to measure pain levels. The present widely used in clinical practice standard measure of pain relief in patients experiencing acute or chronic pain is a change in the numerical rating scale (NRS) score. NRS is a unidimensional scale that requires patients to mark their pain level from 0 (no pain) to 10 (worst pain). The NRS provides practitioners with pain levels pre-and-post treatment and is used as an indication of treatment efficacy. A significant limitation of the NRS, however, is that it provides an estimation of a single dimension of pain, pain intensity. Pain and pain relief, on the other hand, may have many dimensions including pain intensity, duration and magnitude of pain relief. Current multidimensional measures fail to capture duration of pain relief, thus there is a necessity to improve pain assessment tools. The integral of pain relief (IPR) is a novel two-dimensional measure of pain relief and duration of pain relief following treatment and may provide a more accurate depiction of post-treatment pain as well as intervention effectiveness. In this prospective cohort study, we intend to assess the validity of the IPR using validated measures of change in pain intensity (NRS), and the Patients' Global Impression of Change (PGIC) as well as The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) in patients treated with corticosteroid injections for the osteoarthritis of knee joint. The primary objectives of this study include: * Compare pre- and post-treatment scores of the i) IPR dimensions (post-treatment), ii) NRS (pre- and post-treatment), iii) PGIC (post-treatment), and iv) WOMAC (pre- and post-treatment) in patients with knee osteoarthritis treated with intra-articular corticosteroid injections. * Provide preliminary validation for the Integral of Pain Relief as a clinical assessment tool of post-treatment pain relief and treatment efficacy. Secondary objectives of this study include: * Assess whether baseline patient characteristics such as pre-treatment pain intensity score, disease-associated pain duration, age, gender, co-morbidity with diabetes, symptoms of either depression or anxiety, or both, litigation status, occupation, and level of education are important predictors to responses on the four pain outcome measures. * Assess patients' impression of their usage of the daily pain diary versus providing the percentage and duration of pain relief at follow up time points.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Given written Informed Consent to participate in the study
- •Male or female ≥40 years of age
- •Diagnosis of unilateral or bilateral OA of the knee for at least 6 months prior to Screening requiring the use of regular therapies.
- •If bilateral OA exists, pain in the contralateral knee must be less than pain in the index knee as reported by patient
- •Index knee pain on most days (\>15) over the last month
- •Mean score of ≥4 and ≤9 on the 24-hr average pain score (0-10 NRS) using the average daily ratings at least 5 out of 7 days prior to Day 1(Baseline)
- •Have been prescribed and scheduled to receive at least one corticosteroid (triamcinolone) injection to the affected knee
- •Willingness and ability to comply with the study procedures and visit schedules and the ability to follow verbal and written instructions
Exclusion Criteria
- •Lack of signed Informed Consent Form
- •Age less than 40 years old
- •Have any contraindications to administration of corticosteroid medication by intra-articular injection
- •Patients with diagnoses of fibromyalgia, chronic pain syndrome, or other concurrent medical or arthritic conditions which could interfere with the evaluation of the index knee
- •Patients with diagnoses of rheumatoid arthritis, psoriatic arthritis, or any other form of inflammatory arthritis
- •Planned/anticipated surgery in the affected area within 3 months during the study period.
- •Previous intra-articular corticosteroid injection into the index joint within 3 months prior to Screening
- •Concomitant treatment with corticosteroid or other injections into the index joint (e.g. prolotherapy) within 3 months during the study period
- •Concomitant treatment with oral or topical (to the index knee) corticosteroids within 3 months during the study period (except inhaled, intranasal, or topical applied not to the index knee)
- •Any other investigational drug/biologic applied to affected area within 3 months during the study period
Outcomes
Primary Outcomes
Patient's Global Impression of Change (PGIC)
Time Frame: Post-interventional at week 12
Patient's Global Impression of Change (PGIC) scores from Baseline to 12 weeks post-interventional. Patient's Global Impression of Change (PGIC) is a 7-point single item scale ranging from "very much worse" to "very much improved" with "no change" with "no change" at mid-point that evaluated improvement in overall status with treatment during clinical trial.
Integral of Pain Relief (dimensions)
Time Frame: Post-interventional at week 12
Patient's reported percentage (%) and duration of pain relief (days)
Pain Intensity Numeric Rating Scale (NRS)
Time Frame: Baseline, post-interventional at week 12
Change in average daily (24-hr) pain intensity scores (NRS) from baseline to 12 weeks post-interventional. Numeric Rating Scale pain intensity score is recorded daily via pain diary starting from day -7 (one week before baseline). Numeric Rating Scale pain intensity score is recorded daily via pain diary. Numeric Rating Scale is a one-dimensional measure of pain intensity. The pain intensity is rated by participant using a scale from 0 to 10, 0 being the least (no pain) to 10 (worst pain imaginable).
Change in Pain Intensity Numeric Rating Scale (NRS) score
Time Frame: Baseline, post-interventional at week 2
Change in average daily (24-hr) pain intensity scores (NRS) from baseline to 2 weeks post-interventional. Numeric Rating Scale pain intensity score is recorded daily via pain diary starting from day -7 (one week before baseline). Numeric Rating Scale pain intensity score is recorded daily via pain diary. Numeric Rating Scale is a one-dimensional measure of pain intensity. The pain intensity is rated by participant using a scale from 0 to 10, 0 being the least (no pain) to 10 (worst pain imaginable).
Western Ontario and McMaster Universities (WOMAC® 3.1) Osteoarthritis Index
Time Frame: Baseline, post-interventional at week 12
Change in total score from baseline to 12 weeks post-interventional. Western Ontario and McMaster Universities (WOMAC® 3.1) Osteoarthritis Index is a Likert 5 point scale for pain, stiffness and function domains. Activities in each domain are rated by a study participant according to the following scale of difficulty: 0 = None, 1 = Slight, 2 = Moderate, 3 = Very, 4 = Extremely.
Pain Intensity Numeric Rating Scale
Time Frame: Baseline, post-interventional at week 4
Change in average daily (24-hr) pain intensity scores from baseline to 4 weeks post-interventional. Numeric Rating Scale pain intensity score is recorded daily via pain diary starting from day -7 (one week before baseline). Numeric Rating Scale pain intensity score is recorded daily via pain diary. Numeric Rating Scale is a one-dimensional measure of pain intensity. The pain intensity is rated by participant using a scale from 0 to 10, 0 being the least (no pain) to 10 (worst pain imaginable).
Secondary Outcomes
- Use of Analgesic Medication(Baseline, Post-intervention at week 12)
- Patient's Survey(Post-interventional at 12 weeks)