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Protocol N. 2014 - Observational Study on the Quality of Life of Outpatients

Observational Study on the Quality of Life of Patients Attending General Urology, Sexual Medicine, Reproductive Medicine, Uro-oncology, Neuro-urology, Functional Urology Clinics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06193850
Enrollment
10000
Registered
2024-01-05
Start date
2015-02-24
Completion date
2045-01-31
Last updated
2024-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Male Infertility, Sexual Medicine, Urologic Diseases

Keywords

Male Infertility, urology, rare male cancer

Brief summary

Prospective observational study on the quality of life of patients attending general urology, sexual medicine, reproductive medicine, functional urology, neuro-urology and uro-oncology clinics.The data relating to the clinical conditions (disease state, psychological and related to quality of life) of the patients belonging to the above-mentioned clinics will be collected in a specially designed database which will allow us to extract the data in a simple and safe way used for statistical analyses. in clinical research.

Detailed description

The Department of Urology has been engaged for years in the field of medical and surgical research relating to benign and oncological pathologies of the prostate, kidney, excretory tract, testicle, as well as urinary continence and dysfunctions of the sexual and reproductive sphere. The accurate acquisition of clinical and psychometric data before and after any treatment, the follow-up analysis, the attention to the patient's global quality of life (QoL) in relation to the particular organic functions affected by the disease, are at the basis of all the medical advances that can be achieved to guarantee ever better care of the individual's health. In the context of urological clinical practice, outpatient activity plays a fundamental role. This activity, which ranges from general urology to sexual medicine, reproductive medicine, functional urology, neuro-urology and uro-oncology, allows us to come into contact with a large number of patients suffering from the most common uropathologies -andrological . Numerous studies have demonstrated how the treatment and outpatient management of such patients significantly impacts not only the underlying pathology but also their quality of life. The outpatient management of the urological patient ranges from the recognition of the basic pathology to the diagnosis through the request for clinical-laboratory-instrumental investigations, to the possible indication for a medical or surgical treatment and to the follow-up of the patient. The main objectives of this data archive are: 1. Collect clinical, instrumental, laboratory, psychometric and sociodemographic data in patients suffering from a uro-andrological pathology who require a consultation in one of the clinics mentioned above. 2. Collect data on the natural history of the pathologies in question and on the patients' quality of life in order to analyze the predictive factors of persistence and recurrence of symptoms, improvement or worsening of the clinical picture, and possible progression of the disease (both in benign and malignant form) and improve the care and treatment of the patients under examination. 3. Having a follow-up and related studies with a number and above all an extension over time that, to date, is not present in the literature or in any scientific production.

Interventions

OTHERObservation during time

Evaluation through clinical investigation and questionnaires useful for evaluating the patient's psycho-physical conditions

Sponsors

IRCCS San Raffaele
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* subjects belonging to general urology, sexual medicine, reproductive medicine, functional urology, neuro-urology and uro-oncology clinics. * subjects \>= 18 years old * signature of informed consent

Exclusion criteria

* \- subjects \< 18 years * presence of mental or physical disability that may prevent the patient from answering the questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
Sexual function - sexual distressBaseline and up to 6 monthsSexual distress investigated through Sexual Distress Scale questionnaire - SDS (range 12- 48, sexual distress = \> 15).
Sexual function - premature ejaculationBaseline and up to 6 monthsPremature ejaculation investigated through PEDT questionnaire (; Scoring: 0 - 20. \<=8 absence; 9-10 probable; \>=11 premature ejaculation);
Sexual function - male sexual healthBaseline and up to 6 monthsMale sexual health investigated through MSHQ questionnaire (25-item, range: 7 - 80, greater score indicating better function and through Androtest (1 - 32; \> 8 = out of the norm);
Sexual function - androgen deficiencyBaseline and up to 6 monthsAndrogen deficiency in elderly males investigated through ADAM questionnaire (range 10 - 50, 10 = absence and 50 = maximal,
Sexual function - satisfaction with treatment of erection problemsBaseline and up to 6 monthssatisfaction with treatment of erection problems investigated through EDITS questionnaire (range = 0-100; higher scores =more treatment satisfaction),
Female sexual functionBaseline and up to 6 monthsFemale sexual function investigated through Female Sexual Function Index questionnaire - FSFI (range 2 - 36, lower scores = worse sexual functioning),;
Sexual function - Erectile FunctionBaseline and up to 6 monthsSexual function investigated through: International Index of Erectile Function questionnaire IIEF (scoring: 1 - 30 - 6-10: severe; 11-16: Moderate; 17-25: mild; 26-30: absence);

Secondary

MeasureTime frameDescription
Psychological stateBaseline and up to 6 monthsPsychological state investigated through Beck Beck Depression Inventory: Range score 1 - 63; 1-10: normal; 11-16: Mild mood disturbance; 17-20: Borderline clinical depression; 21-30: Moderate depression; 31-40: Severe depression; over 40: Extreme depression.
Prostate function - Incontinence QuestionnaireBaseline and up to 6 monthsIncontinence Questionnaire investigated through ICIQ-SF questionnaire (maximum score of 21; the higher the score, the more severe is the UI, but there is no normal score)
Overactive BladderBaseline and up to 6 monthsOveractive Bladder investigated through OAB-q - Overactive Bladder Questionnaire: the score for each of OAB-q domain are summed and transformed to a score ranging from zero to 100. Higher scores indicate more severe symptoms or better quality of life.
Prostate functionBaseline and up to 6 monthsProstate function investigated through National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) questionnaire: total score range from 0 to 43, three subscales addressing pain (score range 0-21), urinary symptoms (score range 0-10), and quality of life (QOL) (score range 0-12)
Prostate function - Prostatic SymptomsBaseline and up to 6 monthsProstatic Symptoms investigated through IPSS questionnaire International Prostatic Symptoms Score: , Scoring 0 -7, 0-7 mild symptoms, 8-19 moderate symptoms, 20-35 severe symptoms

Countries

Italy

Contacts

Primary ContactAndrea Salonia, MD
salonia.andrea@hsr.it02 2643 5661
Backup ContactAlessia d'Arma, PhD
darma.alessia@hsr.it02 2643 5506

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026