Viewing Study NCT06582173



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06582173
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-30

Brief Title: Mapping the Healthcare Pathway to Multidisciplinary Assessment of 12-25 Year Olds with Somatic Symptom Disorder
Sponsor: None
Organization: None

Study Overview

Official Title: Mapping the Healthcare Pathway to Specialised Multidisciplinary Assessment of 12-25 Year Olds with Somatic Symptom Disorder a Monocentric Descriptive Study Based on Interviews Assisted by a Biographical Grid
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PSOMA
Brief Summary: This study aims to describe the course of successive care events that follow individuals with somatic symptom disorder until they are assessed by a specialized multidisciplinary team Data is collected during interviews with subjects aged 12 to 25 years old accompanied by their parents A biographical grid is used to retrospectively identify all care events that occurred from first symptoms until multidisciplinary assessment Life events and symptoms are collected as well to explore how history of healthcare consumption is linked to other trajectories A qualitative analysis of the recorded interviews aims to describe the subjective experience of this healthcare pathway
Detailed Description: Somatic symptom disorders SSD previously labelled Somatoform disorders are known to challenge healthcare professionals and systems as those common conditions reducing quality of life often lead to excessive referrals and investigations before adequate diagnosis and management Although studies have proved multiple interventions to be effective and cost-effective in various clinical settings little is known about the accurate healthcare utilization associated with SSD Such analysis faces the complexity of SSD detection and labelling due to heterogeneous clinical presentations and disputed cross-disciplinary classifications Even though healthcare is known to be a core theme of patient experience of SSD the investigators lack data describing the trajectory of care and the expectations perceived help and triggering events associated with healthcare services use A better understanding of the healthcare pathway those patients follow will help implement evidence-based treatment effectively

The aim of this study is to trace back the pathway of care that individuals follow before they eventually undergo a specialised multidisciplinary assessment

This descriptive study relies on data retrospectively collected from patients and their parents during face-to-face interviews assisted by a biographical grid Inclusion criteria for patients are to be aged 12 to 25 years old and to be diagnosed with SSD by a specialised multidisciplinary team Variables measured to describe the healthcare pathway are chosen according to professional experience and literature review They are collected alongside concomitant life events both to reduce memory bias and to explore determinants and effects of healthcare consumption as a secondary outcome The subjective experience of this healthcare pathway described by patients and their parents is analysed qualitatively in the verbatim of the audio recorded interview

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None