Comparison · NCT02588664-63cbd1c7
COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based Admissions to Skilled Nursing Facilities (SNF) and Inpatient Rehabilitation Facilities (IRF)
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based Admissions to Skilled Nursing Facilities (SNF) and Inpatient Rehabilitation Facilities (IRF). Trial comparisons, record NCT02588664-63cbd1c7. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02588664-63cbd1c7
On this page
Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.14 | 0.121 | 0.162 | wilson | |
| Risk in group 2 | 0.119 | 0.102 | 0.139 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0213 | -0.00639 | 0.0493 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.18 | 0.952 | 1.46 | log | |
| Odds ratio, group 1 over group 2 | 1.21 | 0.945 | 1.54 | log | |
| Number needed to treat, for one more participant with the outcome on COMPASS Intervention than on Usual Care | 47 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: usual care.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | COMPASS Intervention | Participating hospitals randomized to the intervention will change the structure and process for delivery of post-acute stroke care.~COMPASS Intervention: \*A Post-Acute Coordinator (PAC) will visit each patient prior to discharge from the hospital.~* Patient will receive a follow-up telephone call two days after having been discharged.~* 7-14 days after discharge, the patient will attend post-acute stroke clinic visit and receive an assessment from an Advanced Practice Provider (APP), a brief patient-reported functional assessment to generate an individualized Care Plan, and referrals from an APP. The patient's primary caregiver will be assessed to ensure caregiver availability and ability to support the patient and the caregiver's ability to cope with the new challenges of caregiving.~* Patient will receive a call at 30 and 60 days post-discharge for follow-up of functional status, recovery, risk factor management and their access or utilization of recommended services. | 150 | 1,069 | OG001 |
| Group 2 | Usual Care | Participating hospitals randomized to the usual care group will provide their usual, post-acute stroke care to their patients. | 142 | 1,193 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Subjects With Claims-based Admissions to Skilled Nursing Facilities (SNF) and Inpatient Rehabilitation Facilities (IRF)
- Description
- Time frame
- post-discharge year 1
- Population
- Of the enrolled patients, 2262 were linked to Fee-For-Service (FFS) Medicare claims and included in the analyses.
Source ClinicalTrials.gov
Trial
- Title
- Comprehensive Post-Acute Stroke Services
- NCT number
- NCT02588664
- Phases
- NA
- Conditions
- Stroke, Transient Ischemic Attack
- Interventions
- COMPASS Intervention
- Lead sponsor
- Wake Forest University Health Sciences
- Results first posted
- 2021-06-11
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02588664?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
For software
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT02588664-63cbd1c7