Relative Impacts on Preventative Primary Care--a Longitudinal Evaluation of COVID-19:Phase 1
NCT05813652
Anxiety Disorders, Arthritis
Hamilton, Ontario, Canada
View Trial DetailsNCT Number: NCT02743507
Bundled payment is a new payment reform that encourages health care providers to improve quality and contain costs of care. These arrangements are being rapidly expanded across the country, but evidence about their impact are lacking. This study will use Medicare claims data to evaluate the effect of participation in a large Medicare bundled payment program on the quality and costs of care for common medical and surgical conditions.
This study is active but is not currently recruiting participants.
Notify MeAll sexes
Observational
The overall objective is to examine the effects of the Bundled Payments for Care Improvement (BPCI) Model 2 on the quality and costs of care for conditions related to seven of the ten Medicare severity disease-related groups (MS-DRGs) most commonly selected by program participation. Five of these are surgical (major joint replacement of the lower extremity; double joint replacement of the lower extremity; revision of the hip or knee, hip and femur procedures except major joint; lower extremity and humerus procedure except hip, foot, and femur) and two are medical (simple pneumonia and respiratory infections; chronic obstructive pulmonary disease, bronchitis/asthma). These MS-DRGs represent two larger service lines: orthopedics and pulmonary. For each of these seven MS-DRGs, the team will first describe characteristics of provider organizations participating in bundled payment arrangements, including geographic characteristics and clinical volume. We will subsequently empirically test the effect of bundled payment arrangements on quality outcomes and costs of care for these conditions. Additionally, the team will examine any spillover effects that occur within the service lines that contain these seven MS-DRGs.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Up to 90 days
The study team will analyze changes in unplanned admission rates at 30, 60, and 90 days post-discharge.
Time frame: 12 months
The study team will analyze post-discharge emergency department utilization without re-hospitalization in patients with the specific 10 MS-DRGs to test the effect of bundled payment arrangements on quality outcomes and costs of care for these conditions.
Time frame: 12 months
The study team will analyze all cause mortality in patients with the specified 10 MS-DRGs.
Time frame: 12 months
The study team will analyze total Medicare episode spending for individual patients to test the effect of bundled payment arrangements on quality outcomes and costs of care for these conditions.
Time frame: 12 months
The study team will analyze Medicare spending for initial hospitalization and for services during the initial post-hospitalization period to test the effect of bundled payment arrangements on quality outcomes and costs of care for these conditions.
University of Pennsylvania
Other
The Impact of the Bundled Payments for Care Improvement Program on Quality and Costs of Care
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05813652
Anxiety Disorders, Arthritis
Hamilton, Ontario, Canada
View Trial DetailsNCT01979081
Arterial Occlusive Diseases, Arteriosclerosis
Hamilton, Ontario, Canada
View Trial DetailsNCT01050465
Acne Vulgaris, Acneiform Eruptions
View Trial DetailsNCT06583395
Adnexal Diseases, Amyotrophic Lateral Sclerosis
Palm Desert, California, United States
View Trial Details