The Effect of Changing Angle of Bed on Pain Severity and Vascular Complications Among Cardiac Catheterization Patients

NCT ID: NCT05539092

Last Updated: 2022-09-14

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 82 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-09-30
• Study Completion Date: 2023-02-28

Brief Summary

Care of CVD patients in Egypt is very complex and sensitive because of the high incidence and high mortality rate. In 2019, approximately 18.6 million deaths were attributed to CVD globally. As a consequence, cardiac catheterization remains the criterion standard for evaluation of CAD.

Detailed Description

This study will be conducted in three phases; preparation, implementation, and evaluation.

1. Preparation phase

• Ethical approval will be obtained from the Research Ethics Committee (REC) of the Faculty of Nursing - Mansoura University.
• Content validity of the developed tool will be reviewed by a jury of five experts in the study field and the suggestions of the jury members will be considered.
• The reliability of this tool will be assessed also by using Cronbach's Alpha Test.

2. Implementation phase

• An initial assessment will be carried out for all patients to confirm that they are free from the exclusion criteria.
• Patients will be assigned into two groups: intervention group and control group, 41 patients for each group.
• Before the cardiac catheterization procedure: patients' demographic characteristics and health relevant data will be collected on the first day of admission using part I and part II of tool I.
• In both groups after cardiac catheterization procedure: the sheath will be removed immediately by the nurse.
• In the control group: positioning the patients in supine for 6 hours and the affected leg was straight and immobilized.
• In the intervention group: the researcher will change angle of bed from 15° to 45°.
• The severity of pain will be assessed by using part III of tool I for five times starting immediately after sheath removal.
• Vascular complications monitoring scales will be assessed by using tool III for five times starting immediately after sheath removal.

3. Evaluation phase This phase aims to investigate the effect of changing angle of bed on pain severity and vascular complications for both groups.

Conditions

Cardiac Catheterization

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

intervention group

the researcher will change angle of bed from 15° to 45°. The severity of pain will be assessed for five times starting immediately after sheath removal. Vascular complications monitoring scales will be assessed I for five times starting immediately after sheath removal.

Group Type: EXPERIMENTAL

changing angle of bed

Intervention Type: OTHER

Before the cardiac catheterization procedure: patients' demographic characteristics and health relevant data will be collected on the first day of admission. the researcher will change angle of bed from 15° to 45°.

control group

positioning the patients in supine for 6 hours and the affected leg was straight and immobilized. The severity of pain will be assessed for five times starting immediately after sheath removal. Vascular complications monitoring scales will be assessed I for five times starting immediately after sheath removal.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

changing angle of bed

Before the cardiac catheterization procedure: patients' demographic characteristics and health relevant data will be collected on the first day of admission. the researcher will change angle of bed from 15° to 45°.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

Adult patient ≥ 18 years old of both sexes.

• Conscious patients admitted to the CCU after diagnostic or therapeutic cardiac catheterization.
• Patients who will have femoral artery catheterization.
• Patients who will have normal prothrombin time and partial thromboplastin time.

Exclusion Criteria

• Patients who have previous surgery in the iliac or femoral artery.

• Patients who have chronic back pain.
• Patients who have an active bleed¬ing, hematoma and ecchymosis from insertion site prior to the sheath withdrawal.
• Patient who take anti-coagulant drugs and analgesic therapy within the previous 24 hours before the procedure.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Mansoura University

OTHER

Sponsor Role: lead

Responsible Party

sara sobh mohamed ramadan ellawindy

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

Ref.no.p 0.0237

Identifier Type: -

Identifier Source: org_study_id