Evaluation of information needs regarding sexuality after stoma surgery: a cross sectional study in patients and their partners
Recruiting
- Conditions
- ostomyStoma10013356
- Registration Number
- NL-OMON47779
- Lead Sponsor
- rologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 400
Inclusion Criteria
- Patients who underwent stoma surgery in the past 6 * 24 months at LUMC and HMC
- Partners, if applicable, of patients who underwent stoma surgery in the past 6 * 24 months at LUMC and HMC
- Age older than 18 years
- Patients and/or partners must consent in order to be included in the study
- Ability to understand a questionnaire in Dutch
Exclusion Criteria
- Patients who are mentally incompetent to give informed consent
- Age under 18
- Patients who passed away
- Patients who moved abroad
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- To obtain an insight in the needs and perspectives of patients with a stoma<br /><br>on sexual health care provided by care providers. </p><br>
- Secondary Outcome Measures
Name Time Method <p>- To determine patients* point of view on which care provider should be<br /><br>accountable for providing sexual healthcare<br /><br>- To determine patients* point of view on type and timing of sexual health care<br /><br>- To collect information on partner* perspective and opinions on sexual health<br /><br>care provided by care providers.<br /><br>- To collect information on the influence of having a stoma, sexual<br /><br>dysfunction, and treatment on relationships<br /><br>- To collect information on partners* potential caregiving concerns and<br /><br>productivity loss </p><br>