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COVID-19 - No Health Without Mental Health (Co-COVID-19)

H

Haukeland University Hospital

Status

Completed

Conditions

Covid19
Anxiety

Treatments

Behavioral: Co-mestring (co-coping)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The Corona pandemic is affecting the whole world and since March 12.th 2020 there has been strict qurantene and social isolation interventions in Norway. The aim of this intervention is to reduce the negative and fatal effects of the pandemic. The pandemic and the restrictions that follows it is assumed to affect the mental health of the general population. In this research project we want to examine the use and the effects of a digital self-guided psychological intervention with the aim to increase coping and to reduce psychological problems during and after the pandemic. The participants will be randomized to either an intensive group (new module every 3rd day) or to an ordinary group (new module every 5th day).

Full description

The intervention was developed in a crossdiciplinary and cross-sectorial team within the framework of the research project INTROMAT, an ICT Lighthouse research project funded by the Norwegian Research Council. The content of the digital covid-19 intervention was based on four previously developed digital interventions, all based on systematic user-involvement and user-testing, from our group. The person-based approach inspired the development of the intervention. Based on the research literature and experience from our existing digital interventions we started the development with establishing guiding principles. The intervention consists of 8 modules.

Enrollment

91 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • read and write norwegian
  • above 18 years
  • Mild and moderate stress

Exclusion criteria

  • current treatment for mental health disorders
  • history or present severe mental health disorder

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

91 participants in 2 patient groups

Intensive
Experimental group
Description:
This group recieve access to a new module every 3rd day.
Treatment:
Behavioral: Co-mestring (co-coping)
Ordinary
Experimental group
Description:
This group recieve access to a new module every 5th day.
Treatment:
Behavioral: Co-mestring (co-coping)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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