Mindfulness training before mastectomy to reduce postoperative pain
The Effect of Mindfulness-Based Stress Reduction Training Before Mastectomy on Postoperative Pain in Early Period
This study tests if mindfulness training before mastectomy can help reduce pain and fear of movement after surgery for women with breast cancer.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Istanbul Nisantasi University Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06349395 on ClinicalTrials.gov |
What this trial studies
This research investigates the impact of mindfulness-based stress reduction (MBSR) training delivered through an eight-session program prior to mastectomy on postoperative pain and fear of movement. The study aims to determine if preoperative MBSR can significantly reduce pain levels in patients undergoing mastectomy compared to those who do not receive the training. By focusing on a non-pharmacological approach, the study seeks to enhance patient outcomes and contribute to evolving pain management strategies in breast cancer care. The hypothesis suggests that increased mindfulness may improve pain management and overall quality of life for patients.
Who should consider this trial
Good fit: Ideal candidates are women aged 18 and over who are scheduled for mastectomy and can participate in mindfulness training.
Not a fit: Patients without internet access or those unable to commit to the training schedule may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved pain management and enhanced recovery for patients undergoing mastectomy.
How similar studies have performed: Other studies have shown promising results with mindfulness-based interventions in pain management, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Verbally and in writing agreed to participate in the study after being informed about the research, Are aged 18 and over, Can read, write, and speak Turkish, understand the provided information, and have no issues with verbal communication, Do not have any physical issues that would prevent participation in mindfulness-based stress reduction training, Have not previously received mindfulness-based stress reduction training, Underwent surgery with general anesthesia, Had arterial blood pressure, pulse, oxygen saturation, and body temperature within normal limits during and after surgery, Received non-narcotic and consistent analgesic substances postoperatively for pain control, Were administered antibiotics postoperatively with the same active ingredient. Exclusion Criteria: * Patients without internet access, Those unable to use the application through which the training is provided or without someone to assist them, Individuals who cannot allocate regular time for the training, Patients with chronic pain during the preoperative period who are using analgesics for treatment, Patients with restricted movement activity before the surgery will not be included
Where this trial is running
Istanbul
- Istanbul University - Cerrahpasa — Istanbul, Turkey (Recruiting)
Study contacts
- Study coordinator: Buse Ayyıldız, PhD(c)
- Email: b_seayyildiz@hotmail.com
- Phone: 5533529695
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.