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Psychological Well-being of Patients Awaiting for Cardiac Surgery During the COVID-19 Pandemic

Effect on the COVID-19 Pandemic-induced Reduction in Elective Surgery on Medical Events and Psychological Well-being of Patients Waiting for Cardiac Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04406181
Enrollment
200
Registered
2020-05-28
Start date
2020-05-18
Completion date
2021-01-01
Last updated
2020-06-01

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

Conditions

Anxiety and Fear, Anxiety Depression, Anxiety Postoperative, Psychological Stress

Keywords

cardiac surgery, postoperative consultation, postponed elective surgery, COVID-19

Brief summary

The effect and impact of postponing cardiac surgery / creating a waiting list as a result of COVID-19 on patients, both psychologically and symptomatically on three groups of patients: 1. The degree of anxiety and/or depression induced by their altered medical care trajectory. 2. The incidence of medical problems induced by deferred elective surgery or delayed postoperative ambulatory visit 3. The occurrence of reduced access to medical and psychological help

Detailed description

A prospective study by means of a questionnaire, specifically designed for each of the three groups. 1. Adult patients whose operation date has been deferred 2. Patients who did not have had an operation date 3. Patients who have been operating on during the month before Each group will receive a twofold questionnaire: Part I: Hospital Anxiety and Depression Scale (HADS), a robust questionnaire used for hospitalized and non-hospitalized patients gauging the degree of anxiety and/or depression, irrespective of their specific medical condition. All three groups receive the same list of questions. -Part II: a questionnaire made up specifically for issues concerning the medical/psychological/access aspects during the COVID-19 outbreak. Each of the three groups will receive a questionnaire, adapted to the group they are assigned to. The questionnaires will be delivered by the use of Qualtrics or on paper. Timing and mode of presentation (Qualtrics or fill-in paper on admission) of the questionnaire will depend on the length of the quarantine measures.

Interventions

BEHAVIORALHADS

Hospital Anxiety and Depression Scale

BEHAVIORALa survey

made up specifically for issues concerning the medical/psychological/access aspects during the COVID-19 outbreak

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

All adult patients whose operation date has been deferred due to the pandemic COVID-19. All patients who did not have had an operation date before the pandemic COVID-19. All patients who have been operating on during the month before the pandemic COVID-19.

Exclusion criteria

N/A

Design outcomes

Primary

MeasureTime frameDescription
Anxiety/depression by means of Hospital Anxiety and Depression Scale (HADS)10 minutesThe degree of anxiety and/or depression in all three groups, induced by their altered medical care trajectory. 0-7 = Normal 8-10 = Borderline abnormal (borderline case) 11-21 = Abnormal (case)
Medical problems induced by deferred elective surgery or delayed postoperative ambulatory visit10 minutesThe incidence of medical problems induced by deferred elective surgery or delayed postoperative ambulatory visit by means of an adjusted survey.
Reduced access to medical and psychological help10 minutesThe occurrence of reduced access to medical and psychological help by means of an adjusted survey.

Countries

Belgium

Contacts

Primary ContactVeerle Van Mossevelde, Data Nurse
veerle.vanmossevelde@uzbrussel.be+3224763134

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026