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Neuro-Hope Study: Evaluating psychosocial burden and subjective Disease Expectations in Neurological disorders

Neuro-Hope Study: Evaluating psychosocial burden and subjective Disease Expectations in Neurological disorders - Neuro-Hope Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00036414
Enrollment
2400
Registered
2025-04-01
Start date
2025-04-14
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

MS patients, stroke patients, dementia patients, epilepsy patients

Interventions

Group 1: In accordance with the study's protocol, patients diagnosed with a neurological condition (e.g. stroke, dementia, epilepsy or multiple sclerosis) will be administered a series of questionnair

Sponsors

Klinik fu¨r Psychiatrie, Psychotherapie und Psychosomatik, Universitätsmedizin Frankfurt
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Consecutive inclusion of patients in the Department of Neurology and the Department of Psychiatry, Psychosomatics and Psychotherapy at University Hospital Frankfurt o Legal age o Consent to participate in the study o Patients with a neurovascular disease o Patients with epilepsy o Patients with a neuroimmunological disease o Patients with a dementia

Exclusion criteria

Exclusion criteria: Exclusion Criteria: o Cognitive impairments to such an extent that they influence the patient's ability to give informed consent to participate in the study and to participate in the study feasibility o Severe comprehension difficulties in the German language o Illiteracy o Known schizophrenia or florid delusional disorder not related to the current neurological disease

Design outcomes

Primary

MeasureTime frame
???The examinations are conducted at four distinct measurement points: firstly, during the inpatient stay, and subsequently at three, six and 12 months following discharge. During the initial survey, conducted during the inpatient stay, additional clinical data is collected. At the subsequent measurement points, the sole element administered is the questionnaire package.

Secondary

MeasureTime frame
Screening of psychosocial distress

Countries

Germany

Contacts

Public ContactSimone DSouza

Klinik fu¨r Psychiatrie, Psychotherapie und Psychosomatik, Universitätsmedizin Frankfurt

simone.dsouza@unimedizin-frankfurt.de+496963015079

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026