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Progressive Relaxation Exercises Before Mobilization:Effects on Pain, Anxiety and Physiologic Parameters CABG Patients

The Effect of Progressive Relaxation Exercises Applied Before Mobilization on Pain, Anxiety and Physiological Parameters in Patients With Coronary Artery Bypass Graft Surgery

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06726239
Enrollment
68
Registered
2024-12-10
Start date
2024-05-31
Completion date
2025-06-30
Last updated
2025-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Coronary Artery Bypass Graft Surgery (CABG), Mobilization, Pain, Physiological Parameter, PROGRESSIVE MUSCLE RELAXATION EXERCISES

Keywords

coronary artery bypass graft surgery, pain, Anxiety, progressive relaxation exercise, physiological parameter

Brief summary

This study is planned as a randomized controlled experimental study to determine the effect of progressive relaxation exercises applied before mobilization on pain, anxiety and physiological parameters in patients undergoing coronary artery bypass graft surgery.

Detailed description

This study was planned as a randomized controlled experimental study to determine the effect of progressive relaxation exercises on pain, anxiety and physiological parameters before mobilization in patients undergoing coronary artery bypass graft (CABG) surgery. Ethics committee and institutional approval were obtained before starting the study. Patients were informed about the study and their verbal and written informed consent was obtained. The study will be conducted in a public hospital in Istanbul with 68 patients (experimental group = 34, control group = 34) who met the research criteria and underwent CABG surgery. The patients in the experimental group will be given progressive relaxation exercises twice at 6-hour intervals on postoperative day 1 and day 2. Patients in the control group will receive routine treatment and care. Physiological parameters, pain, and anxiety levels will be evaluated twice daily on postoperative days 1 and 2 in both groups.It was also stated that a smart wristband should be worn on the arms of the patients on postoperative days 1 and 2 to monitor the frequency of mobilization in both the experimental and control groups. In addition, the frequency of analgesic use will be monitored.

Interventions

OTHERProgressive relaxation exercises

The aim of relaxation exercises is to help individuals recognize the difference between tension and relaxation and to enable them to relax in situations of stress. These exercises are performed with light background music and verbal instructions, allowing patients to mentally focus on the process. The progressive relaxation technique involves the voluntary contraction and subsequent relaxation of muscle groups, typically starting from the hands and progressing to the feet, with each muscle group activated in sequence. During the exercise, the instructions and steps from the 'Relaxation Exercises' CD published by the Turkish Psychologists Association will be followed.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Intervention model description

experiment-control

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Ability to read and write in Turkish, * Analgesics given ≥4h before assessment, * Conscious and communicative, * Elective coronary artery bypass graft surgery planned, * Patients undergoing coronary artery bypass graft surgery for the first time were included in the study.

Exclusion criteria

* Diagnosed with a psychiatric or neurological disorder, * Diagnosis of a musculoskeletal condition that could affect mobilization, * Patients with hearing and vision loss, * Patients participating in another clinical trial during the same period, * Patients who developed any complications during the postoperative period were excluded.

Design outcomes

Primary

MeasureTime frameDescription
Descriptive Characteristics FormPreoperativeThe first part includes questions about demographic characteristics such as gender, age, body mass index (height-weight), marital status, education level, income level and occupation, and the second part includes questions about other chronic diseases, previous surgery, previous stay in the intensive care unit, smoking and alcohol use.
Physiological parameters monitoringPostoperative Day 1:(measured twice, 6-hour apart): Control: Pre-test, 30 min later, 15 min post-mobilization Experimental: Pre-test, 5 min post-PGE, 15 min post-mobilization. Postoperative Day 2: Both groups:Same measurements at 6-hour intervals, twicePhysiological parameters will be monitored.
State Anxiety InventoryPostop Day 1:(measured twice, 6-hour apart): Control: Pre-test,30 minutes after,15 min post-mobilization.Experimental: Pre-test, 5 minutes after PGE, 15 min post-mobilization.Postoperative Day 2: Both groups:Same measurements at 6-hour intervals, twiceIt is used to determine how the individual feels right now and the items of the scale are scored between 1-4 points (1=not at all, 2=somewhat, 3=very much, 4=completely).
Short Form McGill Pain QuestionnairePostop1:Measured twice at 6h:Control:Pre-test, 30 min later, post-mobilization vas, 15 min post-mobilization. Experimental: Pre-test, 5 min post-PGE, post-mobilization vas, 15 min post-mobilization.Postop2: Both groups:Measured twice at 6-hour intervalsThe scale consists of three parts in which the nature of pain, intensity of pain and overall pain intensity are evaluated.
Trait Anxiety InventoryPreoperativeThe Trait Anxiety Inventory is used to determine how the individual usually feels and the items of the scale are scored between 1-4 points (1=almost never, 2=sometimes, 3=very often, 4=almost always). There are 7 reversed statements in the trait anxiety subscale (items 21, 26, 27, 30, 33, 36 and 39).

Secondary

MeasureTime frameDescription
Analgesia monitoring formPostoperative day 1 and 2In this form prepared by the researcher in line with the literature, the name, dose, time and route of administration will be recorded in case of analgesic use of the patients.
Mobilization SchedulePostoperative day 1 and 2Mobilization will be assessed on postoperative days 1 and 2 based on the number of steps taken, distance covered, and relevant features of the mobilization process.

Countries

Turkey (Türkiye)

Contacts

Primary ContactTuğçe Bozkurt
tgcebzkrt55@gmail.com05063137927
Backup ContactAyfer Özbaş
tgcebzkrt55@gmail.com05063137927

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026