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NCT Number: NCT06582173

Mapping the Healthcare Pathway to Multidisciplinary Assessment of 12-25 Year Olds With Somatic Symptom Disorder

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.

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Key information

Age range

12 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Maison de Solenn Maison des Adolescents, Cochin Hospital

Paris, IDF, 75014, France

Location status: Recruiting

Location contact

Maude LUDOT-GREGOIRE, MD

PRINCIPAL_INVESTIGATOR

Maude LUDOT-GREGOIRE, MD, PhD

CONTACT

[email protected]

+33 1 58 41 24 26

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Criteria relating to the population studied:

  • Age between 12 and 25 years old
  • Diagnosis of somatic symptom disorder and derivatives (DSM 5) after specialized multidisciplinary evaluation by the team of the Maison des Adolescents of Cochin hospital (Maison de Solenn).

Criteria relating to the additional population participating in the research:

  • Being a parent of a subject who has received the diagnosis of somatic symptom disorder and derivatives (DSM 5) after specialized multidisciplinary evaluation at the Maison des Adolescents of Cochin Hospital (Maison de Solenn).

Exclusion criteria

Criteria relating to the population studied:

  • Age less than 12 years or greater than 25 years at the time of assessment,
  • Subject presenting ongoing psychiatric decompensation, that is to say a state of mental health breaking with their baseline state and requiring rapid care which does not allow a research interview to be carried out.

Criteria relating to the additional population participating in the research:

None

Treatment and study plan

Face-to-face interviews assisted by a biographical grid

Other

Face-to-face interviews assisted by a biographical grid.

Healthcare event of the adolescent :

  • medical specialist appointment
  • general practitioner appointment
  • emergency services use
  • hospital admission
  • diagnostic test
  • medication use
  • non-pharmacological treatment
  • nursing or physical therapy
  • alternative care

Biographical of the adolescent :

  • Education event
  • Class/level
  • School
  • Attendance
  • Special arrangements
  • Grades
  • Off school education
  • Family event
  • Separation/union
  • Birth/death
  • Leave/Arrival
  • Location/Moving
  • Disease/accident
  • Peer events
  • Friendships
  • Love interests
  • Bullying
  • Leisure & interests events
  • Activity
  • Frequency

Primary outcomes

  1. Occurrence of healthcare events

    Time frame: Day of inclusion

    Successive healthcare events of individuals with somatic symptom disorder, from first symptoms to specialised multidisciplinary assessment

Secondary outcomes

  1. Raise of healthcare events occurrence

    Time frame: Day of inclusion

    Raise of healthcare events occurrence following the occurrence of somatic symptoms.

    From first symptoms to specialised multidisciplinary assessment

  2. Raise of life events occurrence

    Time frame: Day of inclusion

    From first symptoms to specialised multidisciplinary assessment

  3. Decrease of healthcare events occurrence

    Time frame: Day of inclusion

    Decrease of healthcare events occurrence following the occurrence of somatic symptoms.

    From first symptoms to specialised multidisciplinary assessment

  4. Decrease of life events occurrence

    Time frame: Day of inclusion

    From first symptoms to specialised multidisciplinary assessment

  5. Modification of somatic symptoms occurrence

    Time frame: Day of inclusion

    From first symptoms to specialised multidisciplinary assessment

  6. Modification of life events occurrence

    Time frame: Day of inclusion

    Modification of life events occurrence following healthcare. From first symptoms to specialised multidisciplinary assessment

  7. Qualitative analysis of the transcribed interviews

    Time frame: Up to 24 months

    Identification of themes emerging from the qualitative analysis of the transcribed interviews

Study contacts

Contact information is provided by the study sponsor or research team.

Marie BENHAMMANI-GODARD

CONTACT

[email protected]

0033158411190

Maude LUDOT-GREGOIRE, MD, PhD

CONTACT

[email protected]

+33 1 58 41 24 26

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • URC-CIC Paris Descartes Necker Cochin

Registry information

Official study 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

Acronym: PSOMA

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Sep 3, 2024
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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