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Evaluation of an in-app treatment "LoCovFit" for reduction of fatigue severity in Long COVID-19 patients

Evaluation of an in-app treatment "LoCovFit" for reduction of fatigue severity in Long COVID-19 patients - LoCovFit

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00030811
Enrollment
170
Registered
2023-03-08
Start date
2023-05-17
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

Long-Covid, Post-Covid, Post-Acute Sequelae of COVID-19, Long COVID-19 U08 U09 U10

Interventions

Group 1: Patients in care-as-usual with full access to the Fimo Health App - Long Covid for 10 weeks Group 2: Patients in care-as-usual without access to the Fimo Health App - Long Covid

Sponsors

Universität Witten/Herdecke
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: a. Diagnosis of Covid-19 confirmed by a positive PCR test. b. Diagnosis of Covid-19 at least one month ago c. Patients suffer from fatigue as measured by the Würzburg Fatigue Inventory (WEIMUS) and have a score of 32 or higher d. Over 18 and under 60 years of age e. Sufficient knowledge of German f. A cell phone with Android 5 operating system or iOS 14 or higher.

Exclusion criteria

Exclusion criteria: a. The patient has a known psychiatric or somatic illness that may explain the fatigue. b. The patient is currently participating in a multidisciplinary rehabilitation program to alleviate the effects of COVID-19

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the severity of fatigue as measured by the Fatigue Severity of the Checklist Individual Strength (CIS) questionnaire. The survey is conducted via an online platform at the beginning of the study (baseline), as well as after the end of the intervention (after 10 weeks).

Secondary

MeasureTime frame
The secondary endpoint is health-related quality of life (HRQL), measured with the Short-Form-36 (SF-36). Another secondary endpoint is the health literacy of the patients. Health literacy is assessed based on eight questions of the EU-HLS-47. The survey is conducted via an online platform at the beginning of the study (baseline), as well as after the end of the intervention (after 10 weeks).

Countries

Germany

Contacts

Public ContactTim Fellerhoff

Fimo Health GmbH

tim.fellerhoff@fimo.io+491707883760

Outcome results

None listed

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