Improving sexual life for patients with Multiple Sclerosis and spinal injuries
Pilot Study on EEG and Behavioral Effects of Two Different Treatments on Sexual Life
This study is testing whether mindfulness and sexual therapy can improve the sexual and emotional lives of people with Multiple Sclerosis and spinal injuries.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | IRCCS San Camillo, Venezia, Italy Academic / other |
| Locations | 1 site (Venice) |
| Trial ID | NCT05142111 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of two different treatments, mindfulness and sexual therapy, on the sexual and sentimental lives of patients with Multiple Sclerosis and spinal cord injuries. Participants will undergo these treatments while their behavioral responses are assessed through questionnaires and brain activity is monitored using high-density electroencephalograms. The goal is to determine the efficacy of these interventions in enhancing the quality of life for individuals facing sexual disorders due to their neurological conditions.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with Multiple Sclerosis or spinal cord injuries who can provide informed consent.
Not a fit: Patients with other significant neurological or psychiatric conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve the sexual health and overall quality of life for patients with neurological disorders.
How similar studies have performed: While there is limited research specifically targeting these treatments in this population, similar approaches have shown promise in improving quality of life in other contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * medical diagnosis of MS or spinal injury. * ability to sign informed consent. Exclusion Criteria: * other relevant previous neurological or psychiatric pathologies.
Where this trial is running
Venice
- IRCCS San Camillo — Venice, Italy (Recruiting)
Study contacts
- Principal investigator: Daniele Marinazzo, PhD — Investigator
- Study coordinator: Giorgio Arcara, PhD
- Email: n.ricercaclinica@ospedalesancamillo.net
- Phone: +390412207594
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.