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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age35-65
SponsorIstanbul University - Cerrahpasa

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Ability to read and write in Turkish,

Analgesics given ≥4h before assessment,

Conscious and communicative,

Elective coronary artery bypass graft surgery planned,

Disqualifiers

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,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Progressive relaxation exercises

    Other intervention

    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.

Treatment groups

68 Participants
are divided into 2 treatment groups
Group A: No InterventionNo intervention 0 interventions
Group B: ExperimentalExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Descriptive Characteristics Form

The 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.

Time frame
Preoperative
2

Trait Anxiety Inventory

The 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).

Time frame
Preoperative
3

Physiological parameters monitoring

Physiological parameters will be monitored.

Time frame
Postoperative 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, twice
4

State Anxiety Inventory

It 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).

Time frame
Postop 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, twice

Secondary outcomes

1

Mobilization Schedule

Mobilization 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.

Time frame
Postoperative day 1 and 2
2

Analgesia monitoring form

In 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.

Time frame
Postoperative day 1 and 2

Other outcomes

Sponsors and contacts

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