Mindfulness-based approach to reduce chronic pain and improve drug therapy
Mindfulness-based Stress Reduction or Usual Treatment for Treatment of Chronic Pain in an Italian Hospital
This study tests if a mindfulness program can help people with chronic pain who are also taking medication feel better and manage their pain more effectively.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Sex | All |
| Sponsor | Azienda Socio Sanitaria Territoriale di Lecco Academic / other |
| Locations | 1 site (Lecco) |
| Trial ID | NCT05843409 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of Mindfulness-Based Stress Reduction (MBSR) in patients suffering from chronic pain who are also undergoing pharmacological treatment. The intervention consists of eight group sessions, each lasting one and a half to two hours, conducted over a period of twelve months. The aim is to enhance patients' awareness and emotional management through mindfulness practices, potentially improving their pain management and overall well-being. The study is conducted virtually, making it accessible to participants during and after the COVID pandemic.
Who should consider this trial
Good fit: Ideal candidates for this study are patients currently receiving pharmacological treatment for chronic pain.
Not a fit: Patients with chronic pain who are not undergoing any pharmacological therapy will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management and quality of life for patients with chronic pain.
How similar studies have performed: Other studies have shown promising results with mindfulness-based interventions for chronic pain, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients being treated for Chronic Pain * Patients with Chronic Pain in Pharmacological Therapy Exclusion Criteria: * Patients with Chronic Pain not in Pharmacological Therapy * Patients without Chronic Pain
Where this trial is running
Lecco
- ASST Lecco — Lecco, Italy (Recruiting)
Study contacts
- Principal investigator: Vincenzo Damico — Rn PhD, Department of Anesthesia and Critical Care, Asst Lecco
- Study coordinator: Vincenzo Damico
- Email: vi.damico@asst-lecco.it
- Phone: +39 3409297118
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.