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VISIT STROKE - Effectiveness of telemedicine rounds in inpatient stroke care

VISIT STROKE - Effectiveness of telemedicine rounds in inpatient stroke care - VISIT STROKE

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00028671
Enrollment
523
Registered
2022-09-27
Start date
2022-10-06
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

G45 I60 I61 I62 I63 I64

Interventions

Group 1: Medical care by neurologist onsite (routine care) Group 2: Medical care by neurologist via telemedicine (intervention)

Sponsors

Charité Campus Benjamin Franklin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients =18 years of age who are undergoing inpatient treatment due to an acute stroke (time from symptom onset to admission <72 h) (ischemic or hemorrhagic stroke, suspected ischemic or hemorrhagic stroke, and suspected transient ischemic attack) and who have already undergone an initial neurological consultation during admission. The initial consultation may have been an on-site consultation or a telemedical consultation. A further inclusion criterion is the consent to study participation by the patient himself or his legal guardian.

Exclusion criteria

Exclusion criteria: Patients who themselves or their legal guardians do not consent to study participation are not included. Time from symptom onset to hospital admission =72h.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the overall correct medical assessment of tele-consultations or on-site consultations in 6 predefined quality indicators: - Etiologic classification - Neurological findings - Risk assessment/detection of complications - Recommended secondary prevention measures - Recommended diagnostic measures - Recommended allied health professional therapies (physiotherapy/language and speech therapy/occupational therapy) and rehabilitative measures The ratings for each indicator result in binary choices (correct/wrong). Only for 6/6 quality indicators rated as correct, the medical assessment in its entirety is considered correct (=primary endpoint). The assessment regarding correctness of the ratings is performed by blinded reviewers.

Secondary

MeasureTime frame
Secondary outcomes are correct medical assessment in the respective 6 quality indicators considered individually. The ratings in the respective quality indicators are considered individually and the corresponding results of the tele-consultations are compared with the on-site consultations. Other secondary outcomes are completeness and accuracy of the medical assessment, which are assessed by the raters using an ordinal scale.

Countries

Germany

Contacts

Public ContactClaudia;Annegret Gorski;Hille

Charité Universitätsmedizin Berlin;Charité Universitätsmedizin Berlin

claudia.gorski@charite.de;annegret.hille@charite.de030 450 544 516;030 450 560 619

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 6, 2026