The Effects of Benson and Progressive Relaxation Techniques on Pain and Sleep in Lobectomy. (NCT07430176) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
The Effects of Benson and Progressive Relaxation Techniques on Pain and Sleep in Lobectomy.
160 participantsStarted 2026-04-20
Plain-language summary
During lobectomy surgical treatment, thoracotomy is performed on patients, and post-thoracotomy pain is observed. Pain is one of the most common problems in patients and causes serious morbidity. As a result of the pain experienced, changes in sympathetic activity and the release of catecholamines as a result of the stress response lead to many complications, primarily in the cardiovascular, urinary, gastrointestinal, and nervous systems. In addition, pain can cause sleep problems in the patient due to the stress response, and the healing process is negatively affected. The aim of this research is to evaluate the effects of Benson relaxation technique and progressive muscle relaxation exercises on the pain levels and sleep quality of patients who have undergone lobectomy, in relation to the pain and sleep problems experienced in the postoperative period. The main aim of the study is to reveal the effectiveness of these two relaxation techniques in reducing pain and improving sleep quality in the postoperative care process, and to develop recommendations for clinical applications based on the findings obtained.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients aged 18 and over, Patients undergoing planned lobectomy surgery for the first time, Patients without diagnosed sleep problems, Patients who volunteer to participate in the study, Patients whose cognitive level is suitable for progressive relaxation and Benson exercises, Patients without visual, hearing, or speech problems will be included in the study.
Exclusion Criteria:
* Patients with mental health issues, those who are not volunteers to participate in the study, and patients undergoing emergency surgery will not be included.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
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Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.