Clinical trial Recruiting at 1 site Interventional Ages 18 to 69

Outreach medical care for housebound adults with Post-COVID syndrome or ME/CFS

Official title: OutreAch MediCal Care for HousEbound Patients With Post-COVID-19 Syndrome or ME/CFS of Any Cause

Run by Hannover Medical School · NCT07352254 · Data updated 2026-11-12

This project will try home visits and remote assessments to learn the symptoms and care needs of adults who are housebound with Post‑COVID syndrome or ME/CFS.

More ME/CFS trials

Quick facts

Study typeInterventional
Ages18 Years to 69 Years
SexAll
Enrollment100 (estimated)
SponsorHannover Medical School
Academic / other
Locations1 site (Hanover)
StatusRecruiting
StartedJanuary 2026
Main results expectedOctober 2028
Study endsDecember 2028
Registry record updatedJanuary 21, 2026
Trial IDNCT07352254 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–70 who meet the Canadian Consensus Criteria for ME/CFS, have a Bell Score ≤30, and experience post‑exertional malaise lasting more than 14 hours are the intended participants.

Probably not a fit

People with pre‑existing conditions that limit mobility or mental capacity (for example major central nervous system diseases), those under 18 or over 70, or patients who can readily attend clinics are unlikely to benefit from this outreach program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The project deploys a multidisciplinary outreach program combining home visits and telemedicine to characterize clinical features and needs of housebound patients with Post‑COVID syndrome or ME/CFS. Specialists in internal medicine, neurology, and psychosomatic medicine will perform standardized histories, physical and mental assessments, and caregivers will be interviewed. Patients are recruited via primary care physicians, patient groups, social media, and post‑COVID outpatient clinics, and existing diagnostic data will be reviewed to identify mimics. The goal is to generate prevalence estimates and a structured care approach that could be integrated into routine services if effective.

Why it matters

Potential benefit: If successful, this could expand access to specialist diagnosis and tailored care for severely affected housebound patients and support routine implementation of outreach services.

How similar studies have gone: Home‑based assessments for other chronic conditions have shown benefit, but targeted outreach specifically for housebound Post‑COVID/ME/CFS patients is relatively novel and under‑studied.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* ME/CFS according to the Canadian Consensus Criteria
* Bell Score ≤ 30
* Duration of the postexertional malaise (PEM) \> 14 hours
* Age \> 18 years and \< 70

Exclusion Criteria:

\- Pre-existing conditions or comorbidities that have (or could have) led to a restriction of mobility or mental capacity, such as various diseases of the central nervous system.

Where it's running

  • Hannover Medical School
    Hanover, Germany
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Registry for ME/CFS patients in Germany

    This study is creating a large registry to collect health information from people of all ages with ME/CFS in Germany, especially those affected by long-term COVID-19 effects, to help improve understanding and treatment of the condition.

    Recruiting Technical University of Munich · Munich, Bavaria · NCT05778006

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.