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CompletedNCT07839598CABG-OREMUpdated Sep 24, 2026

Individualized Orem-Based Nursing Intervention After Coronary Artery Bypass Grafting

An interventional study of Individualized Nursing Intervention Program Based on Orem's Self-Care Theory and Usual postoperative care in Coronary Artery Bypass Grafting (CABG) Surgery, sponsored by Jerash Private University. Completed at 1 site in Jordan. Per ClinicalTrials.gov, last updated 2026-09-24.

Primary conditionDepressionRegistry: Anxiety DisordersReclassifiedWhy we changed it
Registry
Anxiety Disorders — the first condition term the registry derived for this study.
ClinicalTrials.gg
Depression
Why
  1. The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it.
  2. The study's title name Depression.
Confidence
High: the new condition is named in the study's own title. Of 46 hand-checked studies reclassified this way, 72% were exactly right and 89% in the right disease family; the registry's first term was right for 4% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Jerash Private University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 1 month after the study started (first participant enrolled Aug 2025, registered Sep 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
440
Allocation
Randomized
Sex
All
01

Study summary

This randomized controlled trial will evaluate the effectiveness of an individualized self-care and nursing intervention program based on Orem's Self-Care Theory among patients following coronary artery bypass grafting (CABG). The program is designed to address patients' learning needs, strengthen self-efficacy, promote self-care behaviors and wound-management practices, and improve quality of life while reducing anxiety and depression during postoperative recovery. Participants will be randomly assigned in a 1:1 ratio to either the individualized Orem-based self-care and nursing intervention program in addition to usual care or usual care alone. Outcomes will be assessed at baseline, 3 months, and 6 months after the intervention. The study will be conducted in cardiology departments and cardiac intensive care units of hospitals affiliated with the Jordanian Ministry of Health in Jordan.

Read the detailed description

This prospective, two-group, parallel randomized controlled trial evaluated an individualized self-care and nursing intervention program based on Orem's Self-Care Theory among patients following coronary artery bypass grafting (CABG).

The study was conducted in cardiology departments and cardiac intensive care units (CCUs/CICUs) of hospitals affiliated with the Jordanian Ministry of Health in Jordan. Participants were recruited from August 2025 to February 2026, and follow-up assessments continued for 6 months.

A total of 440 eligible patients were randomly allocated in a 1:1 ratio to either the intervention group or the control group. The intervention group received an individualized Nursing Intervention Program Based on Orem's Self-Care Theory in addition to usual postoperative care, whereas the control group received usual postoperative care. The intervention was designed to address patients' individual learning needs and self-care requirements during recovery following CABG.

The intervention incorporated individualized education and nursing support addressing postoperative recovery, medication management, physical activity and gradual mobilization, dietary and lifestyle recommendations, symptom monitoring, recognition of warning signs and complications, surgical wound care, self-care behaviors, cardiac self-efficacy, psychological adjustment, problem-solving, decision-making, and long-term cardiovascular self-management. Educational content was tailored according to each participant's identified learning needs, self-care difficulties, postoperative symptoms, functional limitations, and barriers to recommended self-care.

Participants were assessed at baseline and at 3- and 6-month follow-up. Study outcomes included postoperative learning needs, self-care behaviors, cardiac self-efficacy, anxiety, depression, wound-management behaviors, and health-related quality of life. The study used standardized assessment instruments, including the Postoperative Learning Needs Scale, a CABG-adapted self-care behavior measure, the Cardiac Self-Efficacy Questionnaire, the Hospital Anxiety and Depression Scale, and the EQ-5D-5L.

The primary longitudinal comparison was based on changes in outcomes over time between the intervention and control groups. Longitudinal outcome data were analyzed using linear mixed-effects models incorporating study group, assessment time, and the group-by-time interaction as fixed effects and participant as a random effect to account for repeated measurements.

02

Conditions studied

  • Coronary Artery Bypass Grafting (CABG) Surgery

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Keywords

  • Coronary artery bypass grafting
  • Orem's Self-Care Theory
  • Self-care
  • Nursing intervention
  • Patient education
  • Wound management
  • Quality of life
  • Anxiety
  • Depression
03

In context

Depression Reclassified

8,577 studies on the registry are indexed under Depression; 1,720 are open to participants now.

This study's enrollment of 440 is above the median of 81 across 7,063 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Jerash Private University is the lead sponsor of 8 studies on the registry; 3 are open to participants now.

Compared within Depression, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Anxiety Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Adults who had undergone coronary artery bypass grafting (CABG).
  2. Clinically stable following surgery.
  3. Able to communicate and complete the study questionnaires.
  4. Willing to provide written .
  5. Access to a telephone to facilitate post-discharge follow-up and communication during the recovery period.

Exclusion criteria

Exclusion Criteria:

  1. Clinical or cognitive conditions that substantially interfered with participation in the individualized self-care program or completion of the outcome assessments.
  2. Major postoperative conditions that could independently influence recovery and self-care performance, including major postoperative complications such as stroke or severe wound infection.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
440 participants (actual)

Study arms

  • Experimental
    Intervention Group

    Participants received an individualized Nursing Intervention Program based on Orem's Self-Care Theory in addition to usual postoperative care. The program was individualized according to patients' learning needs, self-care difficulties and capacity, postoperative symptoms, functional limitations, and barriers to recommended self-care. It addressed postoperative recovery, medication management, physical activity and gradual mobilization, dietary and lifestyle recommendations, symptom monitoring, recognition of warning signs and complications, surgical wound care, self-care behaviors, cardiac self-efficacy, psychological adjustment, problem-solving, decision-making, and long-term cardiovascular self-management.

    Behavioral: Individualized Nursing Intervention Program Based on Orem's Self-Care Theory · Other: Usual postoperative care

  • Active comparator
    Control Group

    Participants received usual postoperative care.

    Other: Usual postoperative care

Interventions

  • BehavioralIndividualized Nursing Intervention Program Based on Orem's Self-Care Theory

    An individualized nursing intervention program based on Orem's Self-Care Theory, provided in addition to usual postoperative care. The program was tailored according to patients' identified learning needs, self-care difficulties and capacity, postoperative symptoms, functional limitations, and barriers to recommended self-care. It addressed postoperative recovery, medication management, physical activity and gradual mobilization, dietary and lifestyle recommendations, symptom monitoring, recognition of warning signs and complications, surgical wound care, self-care behaviors, cardiac self-efficacy, psychological adjustment, problem-solving, decision-making, and long-term cardiovascular self-management.

  • OtherUsual postoperative care

    Participants received usual postoperative care according to the routine care provided at the participating hospitals following coronary artery bypass grafting.

06

What researchers measure

Primary outcomes

  1. Postoperative Learning Needs Scale (PLNS) Overall Score

    Postoperative learning needs measured using the overall score of the Postoperative Learning Needs Scale (PLNS), with a possible score range of 0-65. Higher scores indicate greater postoperative learning needs.

    Time frame: Baseline, 3 months, and 6 months after CABG

Secondary outcomes

  1. CABG-Adapted Revised Self-Care Behaviors Scale (RSCB) Overall Score

    Self-care behaviors measured using the CABG-adapted Revised Self-Care Behaviors Scale (RSCB). The instrument contains 29 items scored from 0 to 5, yielding a possible total score of 0-145. Higher scores indicate more frequent performance of self-care behaviors.

    Time frame: Baseline, 3 months, and 6 months after CABG

  2. Cardiac Self-Efficacy Questionnaire (CSEQ) Overall Score

    Cardiac self-efficacy measured using the Cardiac Self-Efficacy Questionnaire (CSEQ). The 16-item questionnaire is scored from 0 to 4 per item, yielding a total score of 0-64. Higher scores indicate greater cardiac self-efficacy.

    Time frame: Baseline, 3 months, and 6 months after CABG

  3. Hospital Anxiety and Depression Scale (HADS) Anxiety Subscale Score

    Anxiety symptoms measured using the anxiety subscale of the Hospital Anxiety and Depression Scale (HADS). The anxiety subscale contains 7 items and produces a score ranging from 0 to 21, with higher scores indicating greater anxiety symptoms.

    Time frame: Baseline, 3 months, and 6 months after CABG

  4. Hospital Anxiety and Depression Scale (HADS) Depression Subscale Score

    Depressive symptoms measured using the depression subscale of the Hospital Anxiety and Depression Scale (HADS). The depression subscale contains 7 items and produces a score ranging from 0 to 21, with higher scores indicating greater depressive symptoms.

    Time frame: Baseline, 3 months, and 6 months after CABG

  5. Wound-Management Behaviors Score

    Wound-management behaviors measured using the wound-related items of the CABG-adapted Revised Self-Care Behaviors Scale (RSCB). The derived wound-management score ranges from 0 to 15, with higher scores indicating more frequent performance of wound-management behaviors.

    Time frame: Baseline, 3 months, and 6 months after CABG

  6. EQ-5D-5L Health-Status Visual Analogue Scale (VAS) Score

    Self-rated health status measured using the EQ-5D-5L visual analogue scale (VAS), recorded on a 0-100 scale. Higher scores indicate better self-rated health status.

    Time frame: Baseline, 3 months, and 6 months after CABG

  7. Study-Derived EQ-5D-5L Dimension-Sum Score

    Health status summarized using the study-derived EQ-5D-5L dimension-sum score. The five EQ-5D-5L dimension levels were summarized as a score ranging from 5 to 25. This score is study-derived and is not a preference-based EQ-5D-5L utility index; higher or lower values should be interpreted according to the scoring procedure used in the study.

    Time frame: Baseline, 3 months, and 6 months after CABG

07

Study locations

1 site
  • Jerash University
    Amman, Dours 009627, Jordan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07839598
Lead sponsor
Jerash Private University
Responsible party
JAWAD AHMAD ABU-SHENNAR (ASST.PROF.DR, Jerash Private University) — Principal investigator
First posted
Sep 24, 2026
Start date
Aug 1, 2025
Primary completion
Aug 1, 2026
Completion
Aug 1, 2026
Last update
Sep 24, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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