Managing Aftercare for Stroke (MAS): MAS-I - a Cross Sectional Study of Post-rehabilitation Stroke Burden and Patients' Needs

Sponsor
Charite University, Berlin, Germany (Other)
Overall Status
Completed
CT.gov ID
NCT02320994
Collaborator
Prof. Dr. Ian Wellwood (Other), Prof. Dr. Jörg Wissel (Other), NeuroCure Clinical Research Center, Charite, Berlin (Other)
64
1
13
4.9

Study Details

Study Description

Brief Summary

In this first step of the study the investigators will assess the needs, disease burden and current treatments of long-term stroke patients (phase MAS-I).

The ultimate aim of the complete MAS project (MAS I, II & III) is the development of a model of stroke aftercare delivery that can be evaluated to estimate effects in both our local and the wider stroke population.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    After discharge from hospital the current healthcare system in Germany allows considerable flexibility (therefore complexity) of patient access and mobility between multiple care providers in the community setting. The investigators believe this aftercare could be better coordinated by a specialized coordinated stroke aftercare service. Comprehensive coordinated multidisciplinary care is a proven concept with proven benefits in both acute and rehabilitation care provided in stroke units and neurorehabilitation centres. In this study the investigators postulate that a similar coordinated approach to care can be extended to the phase after in-patient rehabilitation has ended (i.e. "long-term management" as opposed to "early supported discharge") for disabled patients with stroke living in the community.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    64 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Cross-Sectional
    Official Title:
    Managing Aftercare for Stroke (MAS): MAS-I - a Cross Sectional Study of Post-rehabilitation Stroke Burden and Patients' Needs
    Study Start Date :
    Nov 1, 2014
    Actual Primary Completion Date :
    Dec 1, 2015
    Actual Study Completion Date :
    Dec 1, 2015

    Arms and Interventions

    Arm Intervention/Treatment
    stroke patients

    post-rehabilitation stroke patients

    Outcome Measures

    Primary Outcome Measures

    1. Prevalence of unmet Needs [once]

      Unmet needs of patients and carers after discharge from Rehabilitation. Score of variables examined (self-reported stroke related need, post-stroke spasticity, post-stroke pain, post-stroke aphasia, neuropsychological impairment, post-stroke depression, post-stroke dementia, inadequate secondary prevention, social care need and carer burden).

    Secondary Outcome Measures

    1. post-stroke checklist [once]

      Evaluation of post-stroke checklist as a valid tool to screen for relevant burden of disease after stroke.

    2. Standard practice evaluation [once]

      Comparison of Standard practice in relation to evidence-based recommendations and current Clinical Guidelines for the management of stroke.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥18 years

    • Participation in one of the previously conducted stroke cohort studies: STRAWINSKI or PREDICT

    • Modified Rankin Score (mRS) recorded as = 1 - 5 (at last follow up during cohort study)

    • Informed consent signed by patient or legal representative

    Exclusion Criteria:
    • Unwilling to have pseudonymised data stored, analyzed & anonymously published.

    • Patients participating in the previous studies recruited in centres outside Berlin

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Charité - Universitätsmedizin Berlin (Center for Stroke Research Berlin CSB & NeuroCure Clinical Research Center) Berlin Germany 10117

    Sponsors and Collaborators

    • Charite University, Berlin, Germany
    • Prof. Dr. Ian Wellwood
    • Prof. Dr. Jörg Wissel
    • NeuroCure Clinical Research Center, Charite, Berlin

    Investigators

    • Principal Investigator: Andreas Meisel, Prof. Dr. med., Charité - Universitätsmedizin Berlin, NeuroCure Clinical Research Center & Center for Stroke Research Berlin
    • Principal Investigator: Ian Wellwood, Prof. Dr., Charité - Universitätsmedizin Berlin, Center for Stroke Research Berlin (CSB)
    • Principal Investigator: Jörg Wissel, Prof. Dr., Neurologie und Psychosomatik am Wittenbergplatz

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Andreas Meisel, Prof. Dr. med., Charite University, Berlin, Germany
    ClinicalTrials.gov Identifier:
    NCT02320994
    Other Study ID Numbers:
    • MAS-I
    First Posted:
    Dec 19, 2014
    Last Update Posted:
    Jan 4, 2022
    Last Verified:
    Dec 1, 2021
    Keywords provided by Andreas Meisel, Prof. Dr. med., Charite University, Berlin, Germany
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 4, 2022