CovidResearchTrials by Shray Alag


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Psychoeducational interventionWiki

Developed by Shray Alag
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drug377 Blood sample Wiki 0.33

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D001008 Anxiety Disorders NIH 0.17

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There is one clinical trial.

Clinical Trials


1 Impact of a Minimal Psychoeducational Intervention Versus Standard of Care on Anxiety Among Hospitalized COVID-19 Patients in Denmark: a Randomized Clinical Trial

Background: There is limited knowledge on the psychological implications of COVID-19 among hospitalized patients and their close relatives. Moreover, evidence-based psychological interventions targeting hospitalized COVID-19 patients and their relatives are currently lacking. Objective: To test a minimal psychoeducational intervention versus standard of care for reducing anxiety among hospitalized COVID-19 patients. Methods and analysis: The trial is a Randomized Controlled Trial (RCT) with a 1 month and 3 month follow-up. Hospitalized COVID-19 patients are consecutively included at admission and randomized 1:1 to either an intervention or control group. Patients randomized to the intervention group will receive a minimal psychoeducational intervention just prior to discharge from the hospital. The goal of the intervention is that patients will be prepared and learn to interpret and react to physical and psychological symptoms that are related to recovering from a COVID-19 infection. Data is collected using standardized and validated patient reported outcome measures (PROMs) to assess mental health outcomes. The primary outcome is patient reported anxiety as assess by the Hospital Anxiety and Depression Scale. Perspectives: This study will provide a comprehensive understanding of the psychological implications of the COVID-19 outbreak. If successful, the minimal intervention is easily implemented in daily clinical practice.

NCT04351789 COVID-19 Mental Health Psychoeducation Anxiety Other: Psychoeducational intervention
MeSH:Anxiety Disorders

Primary Outcomes

Description: Anxiety measured by the Hospital Anxiety and Depression Scale. Range in score: 0 - 28. Higher scores = more symptoms of anxiety.

Measure: Anxiety 1 month

Time: 1 month post discharge

Secondary Outcomes

Description: Anxiety measured by the Hospital Anxiety and Depression Scale. Range in score: 0 - 28. Higher scores = more symptoms of anxiety.

Measure: Anxiety 3 months

Time: 3 months post discharge

Description: Depression measured by the Hospital Anxiety and Depression Scale. Range in score: 0 - 28. Higher scores = more symptoms of depression.

Measure: Depression 3 months

Time: 3 months post discharge

Description: PTSD symptoms measured by the Harvard Trauma Questionnaire. Range in score: 16 - 64. Higher scores = more symptoms of PTSD

Measure: Post Traumatic Stress Disorder (PTSD) symptoms 3 months

Time: 3 months post discharge

Description: Anxiety measured by the Hospital Anxiety and Depression Scale. Range in score: 0 - 28. Higher scores = more symptoms of anxiety.

Measure: Anxiety 12 months

Time: 12 months post discharge

Description: PTSD symptoms measured by the Harvard Trauma Questionnaire. Range in score: 16 - 64. Higher scores = more symptoms of PTSD

Measure: Post Traumatic Stress Disorder (PTSD) symptoms 12 months

Time: 12 months post discharge

Description: Depression measured by the Hospital Anxiety and Depression Scale. Range in score: 0 - 28. Higher scores = more symptoms of depression.

Measure: Depression 12 months

Time: 12 months post discharge


No related HPO nodes (Using clinical trials)