Preoperative Pain Neuroscience Education in Patients Undergoing CABG
CompletedNot applicableNCT07783750
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
This randomized controlled trial evaluated the effects of a single preoperative pain neuroscience education (PNE) session on postoperative pain-related outcomes in patients undergoing elective coronary artery bypass grafting (CABG). Participants were randomly allocated to either a PNE group, which received a structured preoperative PNE session in addition to routine preoperative care, or a control group, which received routine preoperative information and care. Outcomes included pain intensity, pain catastrophizing, pain vigilance and awareness, and pressure pain threshold. Assessments were conducted preoperatively and at 24 hours, 1 month, and 3 months after surgery.
Study details
- Official title
- Effect of Preoperative Pain Neuroscience Education on Chronic Postoperative Pain After Coronary Artery Bypass Grafting: A Randomized Controlled Trial
- Conditions
- Coronary Artery Bypass Grafting
- Postoperative Pain
- Interventions
- Sponsor
- İsmail Palalı
- Organization
- Harran University
- Start date
- 2025-06-23
- Primary completion
- 2026-08-03
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: Adults aged 18 years or older Scheduled for elective coronary artery bypass grafting (CABG) through median sternotomy Able to understand and communicate sufficiently to participate in the education and outcome assessments Provided informed consent to participate in the study Exclusion Criteria: Emergency CABG surgery Concomitant cardiac surgical procedures other than CABG Inability to understand or participate in the pain neuroscience education session Cognitive or communication impairment preventing completion of study assessments Postoperative clinical conditions preventing participation in the planned assessments
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07783750