Effect of Position on Back Pain and Comfort After Angiography

NCT ID: NCT06844682

Last Updated: 2025-02-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 130 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-05
• Study Completion Date: 2024-02-28

Brief Summary

After coronary angiography, back pain and comfort levels were measured while the intervention group was positioned and the control group was not positioned

Detailed Description

Patients were assigned to the control and intervention groups by the minimization method. Data were collected using the Visual Analog Scale (VAS) and a Patient Introduction Form to assess the pain and comfort levels of the patients. Prior to the starting the research, the necessary permissions were obtained from the institution where the study was conducted, from the patients and the ethics committee. In the analysis of data, frequency and percentage values, Kolmogorov-Smirnov test for the normal distribution of continuous variables, chi-square for comparisons of qualitative variables, two-way analysis of variance for comparison of repeated measurements of pain and comfort scores according to groups, and the relationship between two continuous variables were evaluated with the Pearson correlation coefficient. p<0.05 was considered statistically significant. IBM SPSS Statistics 23 package program was used for the analysis of the date. The intervention group was hospitalized in supine position after coronary angiography. The first measurement was taken when the patient was placed in bed after the procedure, and the Patient Introduction Form and VAS for comfort and pain were applied (Hour 0). Following the withdrawal of the mattresses, the patient was given the semi-fowler position. VAS was applied at the 2nd and 4th hours after the positioning. Patients in the control group were placed to bed in the supine position in accordance with the routine practice of the clinic at the exit of coronary angiography and were allowed to stay in this position for six hours. When the patients were put to in bed, the Patient Introduction Form, VAS were applied for comfort and pain (0. hour). VAS was applied at the 2nd and 4th hours following the removal of the mattresses. Patients' back pain and comfort were evaluated, and the results were recorded on the relevant forms.

Conditions

Coronary Angiography

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

control group

At the end of CAG, the patients were laid in the supine position in line with the routine practice of the clinic and were allowed to remain in this position for 6 hours. While lying in bed, the patient identification form and VAS for comfort and pain were applied (Hour 0). VAS was applied at the 2nd and 4th hours following the removal of the mattresses. The patients' back pain and comfort were evaluated and the results were recorded on the relevant forms.

Group Type: NO_INTERVENTION

No interventions assigned to this group

intervention group

After CAG, the patients were placed on the bed in the supine position. The first measurement was taken when he was put to bed after CAG, and the patient introduction form and VAS for comfort and pain were applied (0th hour). Following the removal of the mattresses, the patient was placed in the semi-fawler position. VAS was applied 2 and 4 hours after positioning. The patients' back pain and comfort were evaluated with the given position, and the results were recorded on the relevant forms.

Group Type: EXPERIMENTAL

intervention group

Intervention Type: OTHER

Following the removal of the mattresses, the patient was placed in the semi-fawler position.

Interventions

intervention group

Following the removal of the mattresses, the patient was placed in the semi-fawler position.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Coronary angiography for the first time in the coronary intensive care unit and cardiology clinic
• Volunteer to participate in the study
• Femoral angiography procedure performed
• It created patients who had no obstacle to communication.

Exclusion Criteria

• More than one coronary angiography procedure was performed
• Not volunteering to participate in the study
• Radial angiography procedure was performed
• Having a history of back surgery, existing hernia, or chronic waist or back pain

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 95 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Sanko University

OTHER

Sponsor Role: lead

Responsible Party

Eyüp Fırat

Nurse

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Eyüp FIRAT

Role: PRINCIPAL_INVESTIGATOR

SANKO Üniversitesi

Locations

Eyüp

Gaziantep, şahinbey, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

AIBU-SBF-EF-01

Identifier Type: -

Identifier Source: org_study_id