UnknownNot Applicable

Efficacy of the Unified Protocol for Transdiagnostic Treatment of Emotional Disorders (UP) in People With Post Covid-19 Condition.

Spain60 participantsStarted 2023-01-15

Plain-language summary

The present multiple baseline single case trial will study the efficacy and acceptability of the "Unified Protocol for the Transdiagnostic Treatment of Emotional Disorders" in the treatment of emotional symptomatology and/or emotional disorders in a sample of patients with Post Covid-19 condition.

Who can participate

Age range

18 Years

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: * Belong to the autonomous community of Aragón * Be at least 18 years of age * Have a good understanding of Spanish * SARS CoV 2 infection documented by PCR, Ag test or serology * Persistence of symptoms beyond 12 weeks after acute SARS CoV 2 infection * Emotional symptoms (score equal to or greater than 8 points in anxious symptomatology(OASIS) and/or equal to or greater than 7 points in depressive symptomatology (ODSIS)) and/or diagnosis of Emotional disorder (ED) * Internet access available * Signed informed consent. Exclusion Criteria: * Participating in the trial "Specialized nutritional intervention and rehabilitative treatment for improvement of quality of life in a cohort of patients with post covid-19 condition" * That the symptom(s) already existed prior to acute SARS CoV 2 infection * Receiving psychological and/or pharmacological treatment for a mental disorder at present * Having a diagnosis of severe mental disorder * Active suicidal ideation at the time of evaluation.

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

Sociodemographic data

Timeframe: Pre-treatment

Table of symptoms referred by the patient

Timeframe: Up to 12 months

Overall Anxiety Severity and Impairment Scale (OASIS)

Timeframe: Up to 12 months

Overall Depression Severity and Impairment Scale (ODSIS)

Timeframe: Up to 12 months

Anxiety and related disorders interview (ADIS-5)

Timeframe: Pre-treatment

Adjustment disorders

Timeframe: Pre-treatment

Trial details

NCT IDNCT05581277

SponsorInstituto de Investigación Sanitaria Aragón

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-06-15

View on ClinicalTrials.gov More Emotional Disorder trials

Who can participate

Age range

18 Years

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.

What they're measuring

Sociodemographic data

Timeframe: Pre-treatment

Table of symptoms referred by the patient

Timeframe: Up to 12 months

Overall Anxiety Severity and Impairment Scale (OASIS)

Timeframe: Up to 12 months

Overall Depression Severity and Impairment Scale (ODSIS)

Timeframe: Up to 12 months

Anxiety and related disorders interview (ADIS-5)

Timeframe: Pre-treatment

Adjustment disorders

Timeframe: Pre-treatment