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Cognitive-behavioral Therapy for Mental Disorder in COVID-19 Survivors

Italy140 participantsStarted 2023-04-13

Plain-language summary

The consequences of the Intensive Care Unit and the Covid-19 disease are still uncertain. However, many studies are bringing out often psychological and dramatic consequences for many COVID-survivor patients. Among the ex-covid patients discharged from our Intensive Care Unit and with at least one covid-related psychological consequence, we want to evaluate the effectiveness for long-term consequences of COVID-19 of mindfulness-based stress reduction (MBSR) or usual care.

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Intensive care survivors * Surviving COVID-19 patients * Patients with Chronic Pain Anxiety Depression and/or Insomnia in drug therapy Exclusion Criteria: * Patients with Chronic Pain Anxiety Depression and/or Insomnia NOT in drug therapy * Patients not hospitalized in intensive care for COVID-19

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Chronic pain

Timeframe: 6 months and 1 year

Anxiety

Timeframe: 6 months and 1 year

Depression

Timeframe: 6 months and 1 year

Insomnia

Timeframe: 6 months and 1 year

Trial details

NCT IDNCT05815693

SponsorAzienda Socio Sanitaria Territoriale di Lecco

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-11-30

Contact for this trial

Vincenzo LC Damico, PhD

+39 3409297118 vi.damico@asst-lecco.it

View on ClinicalTrials.gov More Post Acute COVID-19 Syndrome trials

Plain-language summary

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.