Improving sexual health in stroke patients through nursing care
The Role of Sexual Nursing Care in Managing Sexual Dysfunctions in Stroke Patients
This study tests if special nursing care for sexual health can help stroke patients in Italy feel better and improve their relationships compared to standard care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 113 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | IRCCS Centro Neurolesi Bonino Pulejo Academic / other |
| Locations | 1 site (Messina, Italy/Messina) |
| Trial ID | NCT06278363 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of sexual nursing care in addressing sexual dysfunctions among stroke patients in Italy. It involves a randomized clinical trial with two groups: one receiving specialized sexual care and the other receiving standard care, both including the patient's partner. Over six months, various assessment scales are utilized, and four outpatient interventions are administered to measure improvements in body awareness, relational dynamics, and overall quality of life. The study highlights the importance of sexual health as a critical aspect of well-being for stroke survivors.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 to 70 who have experienced an ischemic or hemorrhagic stroke within the subacute phase.
Not a fit: Patients with pre-existing neurodegenerative diseases or significant cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance the sexual health and quality of life for stroke patients and their partners.
How similar studies have performed: While the focus on sexual nursing care for stroke patients is relatively novel, similar studies addressing sexual health in other patient populations have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical and neuroradiological diagnosis of ischemic or hemorrhagic stroke. * Age between 18 and 70 years. * Patients in the subacute phase (1-3 months post-event). Exclusion Criteria: * Pre-existing neurodegenerative diseases (e.g., multiple sclerosis). * Endocrine-metabolic and psychiatric pathologies that may interfere with sexual function. * Global aphasia or other cognitive impairments that hinder active participation in training.
Where this trial is running
Messina, Italy/Messina
- IRCCS Centro Neurolesi Bonino Pulejo — Messina, Italy/Messina, Italy (Recruiting)
Study contacts
- Principal investigator: Provvidenza Tommasello, MsC — IRCCS Centro Neurolesi Bonino Pulejo
- Study coordinator: Rocco Salvatore Calabrò, MD,PhD
- Email: roccos.calabro@irccsme.it
- Phone: +39-090-60128123
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.