- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06757205
Analysis of the Personality Characteristics and Lifestyle of Young People Who Access Psychiatric Outpatient Clinics (APGP)
Analysis of the Personality Characteristics and Lifestyle of Young People Who Access Psychiatric Outpatient Clinics: a Qualitative Study
Considering the growing importance of services psychiatric and psychological for adolescence and adulthood incidence of discomfort expressed in this age group, comes assessed the need to provide adequate and targeted services.
Reasons:
The study aims to evaluate the characteristics and trends of adolescents who access the service, in order to frame the type of discomfort expressed and the expectations with respect to access to the service and the resource base on which it can the therapeutic intervention must be thought out and organised. Furthermore, the study aims to identify the factors that influence the request for help and evaluate the quality of the assistance received, with the aim of improving it effectiveness.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Marianna Mazza
- Phone Number: +390630154122
- Email: mariannamazza@hotmail.com
Study Locations
-
-
Roma
-
Rome, Roma, Italy, 00168
- Fondazione Policlinico Universitario A.Gemelli IRCCS
-
Contact:
- Marianna Mazza
- Phone Number: +390630156196
- Email: mariannamazza@hotmail.com
-
Principal Investigator:
- Marianna Mazza
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria:
- Participants will be selected based on their age between 13 and 21, their availability to sign the informed consent.
Exclusion criteria:
- Patients who do not give their consent are excluded from the study.
- Patients who do not speak fluent Italian or those who due to cognitive and/or thinking characteristics would not be able to understand or complete the questionnaire are also excluded.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Analyze the characteristics of adolescents who access the clinic, both with respect to the discomfort presented and the resources available to them
Time Frame: one year
|
Data analysis through qualitative methods to identify recurring trends and patterns.
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Relate these characteristics to the ways of relating within the family, through meetings that also involve their parents
Time Frame: one year
|
Administration of psychometric scales:
|
one year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Collect useful information to improve the effectiveness and variety of therapeutic paths to be offered to adolescents who consult the clinic and their parents.
Time Frame: one year
|
Administration of psychometric scales:
|
one year
|
Collaborators and Investigators
Investigators
- Principal Investigator: Marianna Mazza, Fondazione Policlinico Universitario A. Gemelli, IRCCS
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 7088
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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