Coping With Covid-19: Loneliness, Self-Efficacy, Social Support, Depression & Anxiety in Patients in Medical Rehab.
Loneliness, Depression, Anxiety, Self Efficacy
About this trial
This is an interventional supportive care trial for Loneliness focused on measuring Loneliness, Depression, Anxiety, Post-COVID, COVID-19, Psych
Eligibility Criteria
Inclusion Criteria:
- patients aged 18 years to no upper limit
- patients were diagnosed with COVID-19
- Non-COVID patients with the need to participate in early rehab
Exclusion Criteria:
- a too high language barrier or dyslexia
- patients with intellectual and cognitive impairment (like primary psychiatric illness, e.g., schizophrenia or dementia, if admitted by means of medical history by a physician or if the score achieved in the cognitive screening by means of the mini-mental-state-examination (MMSE) is 23 or below 23 and no improvement of the cognitive performance is to be expected, e.g. because of an incipient dementia)
Sites / Locations
- Helios Klinikum Berlin-Buch GmbHRecruiting
- Jacobs University Bremen gGmbHRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
Intervention 1: According to DGP
Intervention 2: According to Cacioppo "E.A.S.E."
Care as Usual; Standard psychological Support
For the first group, a psychological intervention for psychoeducational measures and psychosocial support, was designed according to the recommendations of the DGP - Deutsche Gesellschaft für Pneumologie und Beatmungsmedizin e.V. for the rehabilitation of post-COVID-19 patients (DGP, 2020). The interventions start approximately two days after data collection at T0. The second measurement time point (T1) is scheduled at the time of patient discharge after the interventions have been implemented. Only patients who scored 8 or higher on the Hospital Anxiety and Depression Scale (HADS) at admission will participate in the interventions. This psychological intervention will be applied to both groups of patients (non-Covid/Covid patients)
The second intervention was designed after Cacioppo's intervention EASE, for processing loneliness. This psychological intervention will be applied to both groups of patients (non-Covid/Covid patients), too. The interventions start approximately two days after data collection at T0. The second measurement time point (T1) is scheduled at the time of patient discharge after the interventions have been implemented. Only patients who scored 8 or higher on the Hospital Anxiety and Depression Scale (HADS) at admission will participate in the interventions.
The patients receive standard care from the psychologists, as is usual in this unit. No intervention is carried out.