Clinical Trials Directory

Trials / Completed

CompletedNCT06871332

Progressive Relaxation Exercise on Pain, Anxiety and Patient Satisfaction

The Effect of Progressive Relaxation Exercise on Pain, Anxiety and Patient Satisfaction Related to Femoral Sheath Removal: a Randomized Controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
70 (actual)
Sponsor
TC Erciyes University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This single-center, prospective, randomized controlled trial was completed with a total of 70 patients, 35 in each of the intervention and control groups. Data were collected using the Patient Information Form, Visual Analogy Scale and State-Trait Anxiety Inventory. Patients in the intervention group performed progressive relaxation exercise for 20 minutes before femoral sheath removal. The patients in the control group received the standard practice of the clinic.

Detailed description

This study aimed to determine the effect of progressive relaxation exercise (PRE) applied to patients undergoing percutaneous coronary intervention (PCI) on pain, anxiety and patient satisfaction related to femoral sheath removal. This single-center, prospective, randomized controlled trial was completed with a total of 70 patients, 35 in each of the intervention and control groups. Data were collected using the Patient Information Form, Visual Analogy Scale and State-Trait Anxiety Inventory. Patients in the intervention group performed PRE for 20 minutes before femoral sheath removal. The patients in the control group received the standard practice of the clinic.

Conditions

Interventions

TypeNameDescription
OTHERProgressive relaxation exercise groupPatients in the intervention group performed progressive relaxation exercise for 20 minutes before femoral sheath removal.

Timeline

Start date
2023-08-02
Primary completion
2024-04-05
Completion
2024-04-05
First posted
2025-03-11
Last updated
2025-03-11

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06871332. Inclusion in this directory is not an endorsement.