Back-on-Track Studying Early Quality Care
- Conditions
- Musculoskeletal Diseases
- Interventions
- Other: Physical TherapistOther: Primary Care Provider
- Registration Number
- NCT02522923
- Lead Sponsor
- Temple University
- Brief Summary
This study is a randomized controlled trial conducted at two clinical sites. The purpose of this study is to determine whether patients with musculoskeletal injuries do better by seeing a primary care provider first versus seeing a physical therapist first. Target enrollment is 150 subjects.
- Detailed Description
Physical therapists have an important role as initial contact providers for individuals with musculoskeletal disorders. Health care expenditures are on the rise each year in the U.S. and a large proportion is due to musculoskeletal disorders. Despite the rise in spending, there has not been an improvement in outcomes for individuals with musculoskeletal disorders. Furthermore, increased medical spending and utilization could expose patients to iatrogenic harm. Comparative effectiveness studies of different portals of entry would help to determine the most effective pathways for individuals with musculoskeletal disorders to seek care. The purpose of this study is to determine whether patients with musculoskeletal injuries do better by seeing a primary care provider first versus seeing a physical therapist first. Subjects will be enrolled from two sites (Temple University, Philadelphia, PA and Brooke Army Medical Center, San Antonio, TX). Patient self-reported outcomes measures will be collected at baseline and 6 weeks. At 6 months, healthcare utilization will be assessed. The investigators plan to enroll a target sample size of 75 subjects per site (150 total). Descriptive statistics will be computed to characterize the 2 treatment groups with ANCOVA being used to assess differences between treatment groups at 6 weeks, adjusting for baseline values, evaluating the assumption of parallel slopes. The investigators will further investigate sources of systematic differences in response to treatment using methods such as generalized estimating equations and linear mixed effects models. This research will be the first multi-site study to compare effectiveness of these two pathways for individuals with musculoskeletal pain in the U.S. With a growing older adult population, the percentage of individuals who have musculoskeletal pain in the U.S. will only increase over time. This research study is timely and could meet the need for identifying the most effective pathway for individuals with musculoskeletal pain to seek care.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 150
- A patient at Temple University Employee Health, OR, Brooke Army Medical Center.
- Able to speak English sufficiently to understand informed consent
- A patient with a musculoskeletal condition as their primary complaint
- Greater than 18 years old
- Within 90 days (3 months) of either initial musculoskeletal onset or repeat acute recurrence of a previous episode
- Patients have already sought care from provider for their presenting condition for this current episode
- Patients have an insurance plan that requires them to see an outside provider prior to seeing the study providers
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- FACTORIAL
- Arm && Interventions
Group Intervention Description Physical Therapist Physical Therapist Participants randomized to this arm will receive care from a physical therapist first. Primary Care Provider Primary Care Provider Participants randomized to this arm will receive care from a primary care provider first.
- Primary Outcome Measures
Name Time Method Physical function on the 10-item short form PROMIS global health measure 6 weeks
- Secondary Outcome Measures
Name Time Method Patient Satisfaction on a Likert scale 6 weeks Acceptability of Symptom State on the PASS 6 weeks Percentage of Subjects using Over-the-counter or Prescription Medication to Assess Medication Usage 6 weeks Number of Physical Therapy or Medical Appointments or Tests orders as a Measure of Health care utilization 6 months Physical function on the Patient Specific Functional Scale 6 weeks Overall Improvement on the Global Rating of Change 6 weeks Number of Limited or Light Duty Days to Measure Work Status 6 weeks Number of Participants with Adverse Events as a Measure of Safety and Tolerability 6 weeks Presenteeism as Measured by Participation at Work on Likert Scale 6 weeks
Trial Locations
- Locations (2)
Brooke Army Medical Center
🇺🇸Fort Sam Houston, Texas, United States
Temple University Employee Health
🇺🇸Philadelphia, Pennsylvania, United States