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Effect of Position on Back Pain and Comfort After Angiography

S

Sanko University

Status

Completed

Conditions

Coronary Angiography

Treatments

Other: intervention group

Study type

Interventional

Funder types

Other

Identifiers

NCT06844682
AIBU-SBF-EF-01

Details and patient eligibility

About

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

Full 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.

Enrollment

130 patients

Sex

All

Ages

18 to 95 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

130 participants in 2 patient groups

control group
No Intervention group
Description:
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.
intervention group
Experimental group
Description:
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.
Treatment:
Other: intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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