Nurse-Led Self-Management Support After Coronary Artery Bypass Surgery
NCT07930819, Not applicable, Not yet recruiting, University of Jordan
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Nurse-Led Self-Management Support After Coronary Artery Bypass Surgery | ClinicalTrials.gov |
| NCT number | NCT07930819 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 384 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Jordan | ClinicalTrials.gov |
| Conditions | Coronary Artery Disease, Coronary Artery Bypass Grafting (CABG), Depression, Anxiety, Psychological Stress, Readmission, Emergency Visit | ClinicalTrials.gov |
| Interventions | BRIDGE-SM model | ClinicalTrials.gov |
| First posted | 2026-11-12 | ClinicalTrials.gov |
| Last updated | 2026-11-12 | ClinicalTrials.gov |
Registered outcomes 4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Number of Participants With Unplanned Healthcare Utilization (Unplanned Hospital Readmission or Emergency Department Visit) | From hospital discharge through Day 45 after discharge | Composite binary outcome (yes/no). A participant is classified as having the outcome if at least one unplanned hospital readmission or emergency department visit occurs within 45 days after hospital discharge following elective CABG surgery. Events are ascertained through participant self-report during telehealth follow-up and verified by medical record review conducted by an independent reviewer masked to group allocation. Results are reported as the proportion of participants with the outcome in each arm, with relative risk, absolute risk reduction, and number needed to treat. | ClinicalTrials.gov |
| Secondary | Cardiac Self-Management | Day 45 after hospital discharge | Cardiac self-management behavior measured using the Arabic version of the Self-Care of Coronary Heart Disease Inventory (SC-CHDI v3.0), a 23-item self-report instrument rated on a 5-point Likert scale with three subscales: Self-Care Maintenance (9 items), Self-Care Monitoring (7 items), and Self-Care Management (7 items). Each subscale is transformed to a standardized score from 0 to 100; higher scores indicate better self-care, and a score of 70 or above indicates adequate self-care. | ClinicalTrials.gov |
| Secondary | Depression, Anxiety, and Stress Severity | Day 45 after hospital discharge | Psychological distress measured using the Arabic-validated DASS-21, a 21-item self-report instrument with three 7-item subscales: depression, anxiety, and stress. Items are rated from 0 to 3; each subscale score is calculated by summing its items and multiplying by two (range 0-42), and the total score ranges from 0 to 126. Higher scores indicate greater symptom severity. Each subscale is analyzed and reported separately. | ClinicalTrials.gov |
| Secondary | All-Cause Mortality (Safety Outcome) | From hospital discharge through Day 45 after discharge | Binary outcome (yes/no): death from any cause within 45 days after hospital discharge. Confirmed through medical record review and death registry verification, supplemented by telephone contact with next of kin when registry data are unavailable. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 4
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.3.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 4a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
Release trials-2026-11-12-0.3.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.