- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02886741
A Ten-state Cluster-randomized Controlled Trial of the Institute for Health Improvement's Project JOINTS
Evaluation of a Multi-modal Network to Spread an Enhanced SSI Prevention Bundle
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
For Project JOINTS, the evaluation team designed a state-level cluster randomized trial involving five pairs of states selected and matched on characteristics described below. One state from each pair received the 6-month Project JOINTS campaign, while the other state served as a control. To measure changes in the relevant evidence-based practices, RAND conducted a survey of orthopedic surgical staff in all ten states before and after Project JOINTS. The project was reviewed and approved by the RAND Institutional Review Board.
Intervention: Project JOINTS built on the notion of synergistic use of evidence-based practices.14 IHI designed and encouraged implementation of a five-component "enhanced" SSI prevention bundle included three relatively new evidence-based practices and two well-established Surgical Care Improvement Program (SCIP) practices. The three evidence-based practices not consistently implemented by hospitals prior to 2010 were:
- Screen patients for nasal Staphylococcus aureus (SA) carriage and decolonize SA carriers with five days of intranasal mupirocin and CHG bathing (minimum 3 consecutive days of daily use) in the days immediately preceding surgery;
- Instruct patients, regardless of SA carriage, to bathe or shower with chlorhexidine gluconate (CHG) for at least three days before surgery;
- Use an alcohol-containing antiseptic agent for preoperative skin preparation. The campaign recruited state organizations from the RSN developed during the 100,000 Lives and 5 Million Lives Campaigns. The state organizations reached out to hospitals in their states inviting them to participate in the campaign, disseminating information about the campaign and its evidence-based practices, and assisting IHI in publicizing activities described below and in a prior publication.
IHI developed a logic model summarizing how campaign activities were designed to achieve specified goals and this was discussed and refined in collaboration with the evaluation team in order to inform evaluation measures. IHI developed intervention materials (including a "How-to Guide," evidence reviews, a summary of the "business case" for the interventions to prevent SSIs, and tip sheets for surgeons and other providers, and patients and families), created and maintained a project website and email listserv, and offered a range of learning opportunities (including webinar calls, faculty-led office hours, and town hall meetings). Hospital and practice staff who participated in Project JOINTS (typically quality or safety improvement leaders and staff with oversight of infection prevention) received access to a password-protected IHI website maintained by IHI.
In addition to SSI prevention in hip and knee arthroplasty, the Project JOINTs "How To Guide" also addressed important elements of the "Model for Improvement," developed by Associates in Process Improvement and later adapted by IHI for use in its campaigns. These elements included: (1) the development of a QI plan (including explicit aims and a measurement framework); (2) small-scale tests of change- ("PDSA cycles") to refine implementation approaches through iterative learning; and (3) reliance on multi-disciplinary implementation teams. To enhance credibility with clinicians, IHI collaborated with relevant professional organizations, recruiting faculty from the American Academy of Orthopedic Surgeons (AAOS) and the American Association of Hip and Knee Surgeons (AAHKS) and obtaining endorsement from the AAHKS.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Surgeons, nurses, and other staff involved in direct care of patients undergoing hip or knee arthroplasty.
- Staff had to be affiliated with one of 20 hospitals selected at random from among all hospitals in each of 10 states that performed a minimum of 100 hip or knee arthroplasties for Medicare beneficiaries.
Exclusion Criteria:
- Per diem staff
Study Plan
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
OTHER: Quality Improvement Campaign
IHI designed and encouraged implementation of a five-component "enhanced" surgical site infection (SSI) prevention bundle with three relatively new evidence-based practices and two Surgical Care Improvement Program (SCIP) practices. The campaign recruited state organizations to share information about evidence-based practices and publicize IHI activities and intervention materials (a "How-to Guide," evidence reviews, a summary of the "business case" for interventions, and tip sheets for surgeons, other providers, patients and families). A project website and email listserv offered learning opportunities including webinar calls, faculty-led office hours, and town hall meetings. |
"How To Guide" addressed development of a QI plan; small-scale tests of change- ("PDSA cycles") to refine implementation approaches through iterative learning; and reliance on multi-disciplinary implementation teams.
IHI recruited relevant professional organizations to identify faculty.
|
|
NO_INTERVENTION: Comparison
Matched state pairs received no campaign intervention and experienced usual care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adherence to new evidence based practices
Time Frame: 6 months
|
The questions addressed three actions (or subcomponents) constituting the nasal screening and decolonization process (new practice 1): screening for SA (1.a.); mupirocin nasal decolonization for methicillin-resistant SA (MRSA) (1.b.) and mupirocin nasal decolonization for methicillin-sensitive SA (MSSA) (1.c.).
It included a question on skin decolonization using CHG (new practice 2) and a question on alcohol-containing antiseptic in the operating room (new practice 3).
Respondents were asked to indicate the frequency of use of each practice among patients undergoing hip or knee arthroplasty.
Response options ranged from 0 to 100% in 10% increments and a "don't know" option.
The survey separated practices one and two, but these may not be effective if not used together.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adherence to established SCIP practices
Time Frame: 6 months
|
The survey also included questions on evidence-based practices previously promoted by an established SSI prevention program (the Surgical Care Improvement Program or SCIP): a question about initiation of perioperative intravenous antibiotics within the appropriate time interval prior to the start of arthroplasty (4.a.), a question about use of intravenous vancomycin for prophylaxis for patients known to be MRSA carriers (4.b.), and a question on use of appropriate hair removal techniques
|
6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Eric C Schneider, MD, The Commonwealth Fund
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2010-0488-CR05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Disorder of Hip Region
-
Nova Scotia Health AuthorityWithdrawnDisorder of Hip Region
-
Antalya Training and Research HospitalCompletedDisorder of Hip Joint
-
California State University, Dominguez HillsUnknownDisorder of Hip Joint
-
Zagazig UniversityRecruitingDiscitis of Thoracic RegionEgypt
-
University Hospital, GhentCompleted
-
Aegeria Soft Tissue LLCUnknownDisorder of Soft Tissue of Body Wall RegionUnited States
-
Johann Wolfgang Goethe University HospitalCompletedFusion of Spine, Lumbar Region
-
Clinique Saint Jean, FranceRecruitingFusion of Spine, Lumbar RegionFrance
-
National Taiwan University HospitalUnknown
-
Taipei Veterans General Hospital, TaiwanNot yet recruitingOther Fusion of Spine, Cervical Region
Clinical Trials on Quality Improvement Campaign
-
University of Massachusetts, WorcesterBoston University; University of Colorado, Denver; Eunice Kennedy Shriver National... and other collaboratorsNot yet recruitingSUID | Sudden Infant Death Syndrome (SIDS) | Safe Sleep EducationUnited States
-
Institute for Clinical Effectiveness and Health...Inter-American Development BankUnknownColorectal NeoplasmsArgentina
-
Institute for Clinical Effectiveness and Health...Ministry of Public Health, ArgentinaCompletedCardiovascular Diseases | Quality ImprovementArgentina
-
Brigham and Women's HospitalCompletedGestational Diabetes Mellitus
-
Sunnybrook Health Sciences CentreCanadian Institutes of Health Research (CIHR); Heart and Stroke Foundation...Completed
-
Duke UniversityNorthwestern University; Wake Forest University Health SciencesCompletedSickle Cell DiseaseUnited States
-
Dartmouth-Hitchcock Medical CenterConcord Hospital; MGH Multiple Sclerosis Clinic; University of Vermont Multiple... and other collaboratorsCompletedMultiple SclerosisUnited States
-
Lawson Health Research InstituteCanadian Institutes of Health Research (CIHR); AstraZeneca; Canadian Diabetes... and other collaboratorsCompletedType 2 Diabetes MellitusCanada
-
HealthPartners InstituteNovartis; TriHealth Inc.; William Beaumont Hospitals; Advocate Medical Group; Baystate... and other collaboratorsCompleted