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Evaluation of an Internet-based intervention for patients with Long/Post-COVID following acute COVID-19 infection: A randomized controlled trial

Evaluation of an Internet-based intervention for patients with Long/Post-COVID following acute COVID-19 infection: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032199
Enrollment
134
Registered
2023-07-11
Start date
2023-06-27
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

U09.9

Interventions

Group 1: Intervention group (rehabilitation/ outpatients + ReCOVer mobile intervention) Patients of the cooperating rehabilitation center, who fulfill the inclusion criteria, are randomized to the in

Sponsors

TU Dresden
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - fluency in German - Long/Post-COVID diagnosis OR ongoing COVID-19 symptoms, new symptoms as a consequence of COVID-19, deterioration of a pre-existing illnes after COVID-19 - confirmation of COVID-19 diagnosis by a positive COVID-19 PCR test (self-report)

Exclusion criteria

Exclusion criteria: - current psychotic illness - current addiction - missing confirmation of a COVID-19 infection by a positive COVID-19 PCR test - Functional status after Long/Post-COVID: exclusion with level 0 and 1

Design outcomes

Primary

MeasureTime frame
Differences in quality of life between intervention- and control group at post-test. Quality of life is assessed by EQ-5D-5L.

Secondary

MeasureTime frame
1. Minimal Clinically Important Difference in quality of life of at least 15% of the range of the EQ-5D-5L in the intervention group. 2. Differences in psychological symptoms between intervention- and control group at post-test. Psychological symptoms are assessed by PHQ-D. 3. Acceptance, assessed by self-generated questionnaires to evaluate the single chapters and the intervention. 4. Target group/ range of influence, assessed by a self-generated questionnaire about sociodemographic variables. 5. Adherence, assessed by the number of finished chapters of the intervention.

Countries

Germany

Contacts

Public ContactCorinna Jacobi

Technische Universität Dresden

corinna.jacobi@tu-dresden.de+49 351 463-37469

Outcome results

None listed

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