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Tele-neurological outpatient care in Brandenburg and Mecklenburg-Western Pomerania

Tele-neurological outpatient care in Brandenburg and Mecklenburg-Western Pomerania - TENEAM

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00037679
Enrollment
8610
Registered
2025-10-13
Start date
2025-11-10
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

G20-G26 G35-G37 G30-G32 G40-G47 F01 F03 R42 G61 G56 G57 G50

Interventions

Group 1: TENEAM – Intervention arm (according to TIDieR) 1. Name of the intervention Teleneurological care (TENEAM). 2. Why (rationale, theory, goal) Addressing the lack of specialist neurological c
patients do not have to travel to the neurologist themselves. 8. When and how often (dosage, duration) At least one teleneurological consultation per patient as needed, supplemented by additional ses

Sponsors

Charité - Univeristätsmedizin Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: -Unclear neurological symptoms or confirmed neurological diseases requiring specialist neurological assessment or treatment (e.g., balance disorders, peripheral neuropathies, primary headaches, epilepsy, dementia syndromes, movement disorders, cerebral circulatory disorders, inflammatory CNS syndromes; ; ICD-10 Codes G20-26, G35-37, G30-32, G40-47, G50-54, G56-59, G61.1-G61.9, G62-64, G70-72, H8182, R42, F01, F03) -No specialist appointment available in the near future and close to home (= no appointment within 3 weeks at a specialist neurological practice within =30 min. travel time) -Legal age (= 18 years) -Written consent to participate in the study and use of routine data

Exclusion criteria

Exclusion criteria: - Patients receiving care from a family doctor at another practice and referred to the cooperating practice solely on the basis of a practice substitution

Design outcomes

Primary

MeasureTime frame
Number of outpatient-sensitive hospital treatments with neurological diagnoses within 6 months of inclusion in the evaluation (at least one of the defined outpatient-sensitive neurological ICD-10 diagnoses must be present as a confirmed primary or secondary diagnosis, e.g., G20-26, G35-37, G30-32, G40-47, G50-54, G56-59, G61.1-G61.9, G62-64, G70-72, H8182, R42, F01, F03)

Secondary

MeasureTime frame
Outcome quality - Outpatient-sensitive inpatient hospital cases with neurological diagnoses (up to 24 months) - Outpatient-sensitive emergency room cases with neurological diagnoses (up to 24 months) - Outpatient-sensitive hospital treatments with neurological diagnoses (emergency room + inpatient) during the entire observation period (up to 24 months) - Health-related quality of life (EQ-5D-5L) after 6 months - Well-being (ICECAP-A) after 6 months - Patient satisfaction with timely and appropriate neurological care after 6 months - Access to care (subdomain of EPAT-64 outpatient) after 6 months Structural quality - Time from clarification/treatment need to specialist neurological consultation - Number of specialist neurological consultations per patient year (6–24 months) (GP consultations are also taken into account) Process quality - Completion of guideline-based diagnostics within 6 months - Time to completion of guideline-based diagnostics (from randomization) In a random sample evaluation, the following parameters are collected from project participants: - Satisfaction of family doctors with regard to timely and professional neurological care and acceptance of the new form of care (visual analog scale) - Satisfaction of general practitioners with regard to referral and care costs (visual analog scale) - Satisfaction of neurologists in the region with regard to task distribution and involvement (visual analog scale) Structural quality - Time from clarification/treatment need to specialist neurological consultation - Number of specialist neurological consultations per patient year (6–24 months) (GP consultations are also taken into account) In addition, semi-structured interviews with project participants will be conducted to assess • the degree of implementation of the new form of care • the acceptance of the new form of care • barriers and facilitating factors for the new form of care

Countries

Germany

Contacts

Public ContactChristiane Franke

Charité - Universitätsmedizin Berlin

christiana.franke@charite.de+49 30 450 560 833

Outcome results

None listed

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