Dysmenorrhea Clinical Trial
— DEMETEROfficial title:
Monocentric Descriptive Study Regarding the Impact of Severe Dysmenorrhea on Teenagers, Their Parents and Caregivers Receiving Those Patients
Verified date | November 2022 |
Source | University Hospital, Toulouse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Teenagers experimenting severe dysmenorrhea also face age-specific challenges, particularly impacting their self-confidence, self-esteem, and relations. On one hand, the study team will conduct focus group interviews to better understand the experience of teenagers and their parents consulting pediatric services for severe dysmenorrhea. On the other hand, they will conduct focus group interviews with caregivers from services that usually encounter such patients (gastrologic, gynecologic and pain services). This, allowing to later propose specific tools and healthcare organization to evaluate and accompany teenagers suffering from severe dysmenorrhea.
Status | Completed |
Enrollment | 27 |
Est. completion date | September 13, 2022 |
Est. primary completion date | September 13, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 11 Years to 100 Years |
Eligibility | INCLUSION CRITERIA : - For " teenage" groups: - adolescents between 11 and 17 years old - consulting for severe dysmenorrhea (whether through pediatric gynecology, pain management or gastric consultation) - For "parents" groups: o Parent (mother or father) of an adolescent patient consulting for severe dysmenorrhea - For "medical staff" groups: - Member of a consultation receiving adolescent patients with severe dysmenorrhea - All type of professionals (nurses, psychologist, doctors…) Exclusion criteria : - For " teenage" groups: - suffering from an identified chronical disease - identified psychiatric condition - For "parents" groups: o Parents whose adolescent opposes their participation in this study - For "medical staff" groups: - no exclusion criteria |
Country | Name | City | State |
---|---|---|---|
France | Uh Toulouse | Toulouse | Occitanie |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Toulouse | Fondation pour la Recherche Médicale |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | main themes emerging from focus group | qualitative outcome : identifying the main verbatim used during the focus group | up to one year |
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