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Neurodegenerative DisordersJOCONDENCT05394974

Joint Consultation Between a Neurologist and a Clinical Psychologist

An observational study of Neurodegenerative Disorders, run by University Hospital, Strasbourg, France at 1 site in France.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Joint consultations appeared a few years ago in routine medical practice, but they are still not widely used and rarely evaluated. The primary purpose of the study is to evaluate the impact for the patient of the presence of a clinical psychologist during the joint consultation. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Neurodegenerative Disorders
How many people
200 participants
Where
1 siteFrance
Study dates
1 Jun 2021to 1 Jun 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: Adult patient with a neurodegenerative and/or neurogenetic disease

Who may be able to join

  • patient with a neurodegenerative and/or neurogenetic disease
  • adult patient

Who cannot join

  • dementia
  • age <18 years

Trial locations and contacts

1 site in 1 country.

France1 site, 1 recruiting
  • Service de Neurologie - CHU de Strasbourg - France

    Strasbourg, 67091

    Mathieu ANHEIM, MD, PhD, +33388128535, mathieu.anheim@chru-strasbourg.fr

    Mathieu ANHEIM, MD, PhD

    Recruiting

Other trials in France

About this study

Official title: Evaluation of a Joint Consultation Between a Neurologist and a Clinical Psychologist, Dedicated to Neurodegenerative and/or Neurogenetic Disorders

Joint consultations appeared a few years ago in routine medical practice, but they are still not widely used and rarely evaluated.

The primary purpose of the study is to evaluate the impact for the patient of the presence of a clinical psychologist during the joint consultation.

The secondary purpose is to evaluate the impact for the patient and for the neurologist of the presence of a clinical psychologist during the joint consultation

Keywords
Joint neurologist, psychologist consultation, neurodegenerative and/or neurogenetic disease
Medical subject headings
Neurodegenerative Diseases

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Patient satisfaction after the consultation assessed by 3 questions on a Likert scale

    5-point Likert scale from which to select a response :

    1. Very satisfied.
    2. Moderately satisfied.
    3. Neither satisfied nor dissatisfied.
    4. Moderately dissatisfied.
    5. Very dissatisfied.

    Measured: After consultation et 1 to 3 months later

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 May 2022
  2. Study start1 Jun 2021
  3. Primary completion1 Jun 2023 (estimated)
  4. Study completion1 Jun 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05394974
Sponsor's protocol ID
JOCONDE
Acronym
JOCONDE
Status last verified
May 2022
First submitted
23 May 2022
Last updated
13 Jun 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Neurodegenerative Disorders, run by University Hospital, Strasbourg, France at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 13 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Mathieu ANHEIM, MD, PhD (+33 3 88 12 85 35, mathieu.anheim@chru-strasbourg.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Patient satisfaction after the consultation assessed by 3 questions on a Likert scale (time frame: After consultation et 1 to 3 months later). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jun 2022.

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