Cognitive Disengagement Syndrome in Functional Neurological Symptom Disorder
Official title: Symptoms of Sluggish Cognitive Tempo/Cognitive Disengagement Syndrome in Functional Neurological Symptom Disorder/Conversion Disorder: A Cross-Sectional Case-Control Study
Run by Elazığ Mental Health and Diseases Hospital · NCT07451821 · Data updated 2026-11-12
This study tests whether adults with Functional Neurological Symptom Disorder have more sluggish cognitive tempo symptoms than healthy people.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Elazığ Mental Health and Diseases Hospital Government |
| Locations | 2 sites (Elâzığ, Elâzığ and 1 other locations) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | December 24, 2026 |
| Study ends | December 24, 2026 |
| Registry record updated | September 10, 2026 |
| Trial ID | NCT07451821 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–65 with a DSM-5-TR diagnosis of FNSD/CD, in remission, and without comorbid psychiatric or neurological conditions affecting cognition.
✕Probably not a fit
Individuals with active substance use, other psychiatric or neurological conditions affecting cognition, or age outside 18–65 may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This cross‑sectional, case‑control study compares SCT/CDS symptoms in adults with Functional Neurological Symptom Disorder to healthy controls. Researchers will relate SCT/CDS symptoms to clinical features within the FNSD group. The design aims to identify whether SCT/CDS is more prevalent in FNSD/CD and how it correlates with functional impairment or other clinical variables. The study is observational and does not involve an intervention. Participants are adults aged 18–65, with specific exclusion criteria to reduce confounding.
Why it matters
Potential benefit: If successful, findings could improve understanding of cognitive disengagement in FNSD/CD and guide future assessments or targeted supportive strategies.
How similar studies have gone: There is limited prior systematic study of SCT/CDS in FNSD/CD, so this approach explores relatively novel territory.
Who can join: the full rules
Show full inclusion / exclusion criteria
* Inclusion Criteria for the Functional Neurological Symptom Disorder (FNSD) Group: 1. Meeting the diagnostic criteria for FNSD/CD according to DSM-5-TR at the time of admission 2. Being between 18-65 years of age 3. Absence of additional psychiatric disorders 4. Absence of alcohol/substance use disorder 5. Absence of neurological disorders affecting cognition 6. Being in remission with FNSD/CD 7. Completing sociodemographic data fully 8. Willingness to complete the forms and scales. 9. Willingness to participate in the study * Exclusion Criteria for the FNSD Group: 1. Being under 18 or over 65 years of age 2. Not meeting the diagnostic criteria for FNSD/CD according to DSM-5-TR 3. Active alcohol/substance use 4. Having neurological diseases affecting cognitive functions (such as Alzheimer's disease, delirium, Parkinson's disease) 5. Not being willing to participate in the study 6. Incomplete sociodemographic data 7. Not being willing to complete forms and scales. * Inclusion Criteria for the Healthy Control (HC) Group 1. Being between 18-65 years of age 2. Not having any psychiatric disorder 3. Not having an alcohol/substance use disorder 4. Not having a neurological disorder affecting cognition 5. Completing sociodemographic data in full 6. Being willing to complete the forms and scales. 7. Being willing to participate in the study * Exclusion Criteria for the HC Group: 1. Being under 18 or over 65 years of age 2. Having a psychiatric disorder 3. Active alcohol/substance use 4. Having neurological diseases affecting cognitive functions (such as Alzheimer's disease, delirium, Parkinson's disease) 5. Not being willing to participate in the study 6. Incomplete sociodemographic data 7. Not being willing to complete forms and scales.
Where it's running
-
Elazığ Mental Health and Diseases Hospital
Elâzığ, Elâzığ, Turkey (Türkiye) Recruiting -
Elazığ Mental Health and Diseases Hospital Psychiatry Clinic
Elâzığ, Elâzığ, Turkey (Türkiye) Not yet recruiting
Study contacts
- Study coordinator: Mehmet Hamdi ÖRÜM, MD, Assoc Prof, Psychiatrist
- Email: mhorum@hotmail.com
- Phone: +905382207558
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.