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NCT Number: NCT06621758

Communication Regarding Preclinical Dementia Diagnostic and Diagnostic Disclosure Among Patients with MCI and SCD

The study investigate what information individuals with SCD or MCI and their co-participant would like to receive during pre-diagnostic counseling and diagnostic disclosure, and how this information should be conveyed.

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Key information

About this study

Improved diagnostic work-up and the introduction of disease-modifying treatment have led to a shift towards earlier diagnosis. However, there are a need for better understanding of how best to communicate about biomarker use, assessment, and results in individuals with subjective cognitive decline (SCD) and mild cognitive impairment (MCI).

Objective:

The overarching objective of this study is:

To understand what information individuals with SCD or MCI and their co-participant would like to receive during pre-diagnostic counseling and diagnostic disclosure, and how this information should be conveyed.

Methods: a prospective survey study Persons diagnosed with SCD or MCI and co-participants will be recruited consecutively from the memory clinic, Copenhagen University Hospital - Rigshospitalet (Denmark), Toulouse University Hospital, (France), University Medical Centre Ljubljana (Slovenia) and Universitair Ziekenhuis Brussel (Belgium)

Approximately 30 persons and respective co-participants will be included from each hospital over a period of 12 months.

Each participating person and co-participant will be asked to complete a very brief questionnaire immediately after disclosure of the diagnosis, and another questionnaire 2-6 weeks after the disclosure visit.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosed with SCD or MCI
  • Lumbar puncture performed during the diagnostic process
  • Age at or below 80 years
  • MMSE at or above 24

Exclusion criteria

  • Diagnosis of current major psychiatric disorder (schizophrenia, bipolar disorder, psychosis)
  • Current excessive alcohol intake or substance abuse

Inclusion criteria

for the co-participant:

  • Attended the diagnostic disclosure visit together with the individual diagnosed with SCD or MCI

Treatment and study plan

Questionnaire

Other

Questionnaire regarding biomarker counseling and diagnostic disclosure

Primary outcomes

  1. Important issues in communication

    Time frame: From enrollment to the second questionnaire after 6 weeks

    Rating of which issues are important for persons with SCD or MCI and their co-participant in the pre-diagnostic counseling and diagnostic disclosure communication.

Study contacts

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

Kristian S Frederiksen, MD, PhD

CONTACT

[email protected]

+45 35456922

Marie Bruun, MD, PhD

CONTACT

[email protected]

+45 35451910

Sponsors and collaborators

Lead sponsor

Danish Dementia Research Centre

Network

Collaborators

  • Toulouse University Hospital, Department of Geriatric & Internal Medicine, France
  • Universitair Ziekenhuis Brussel, Department of Neurology, Belgium
  • University Medical Centre Ljubljana, Department of Neurology, Slovenia

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Oct 1, 2024
Registry last updated
Oct 1, 2024

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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