Clinical Trials Directory

Trials / Completed

CompletedNCT05956405

Retraining of the Amygdala and Insula for the Treatment of Persistent Covid

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Hospital Miguel Servet · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Prolonged COVID, also known as post-COVID or Sar-CoV-2 infection with post-acute sequelae, refers to a set of multi-organ symptoms that persist in patients who have suffered SARS-CoV-2 infection, even after of the acute phase of the disease. Approximately 10% of people experience this set of symptoms after their acute COVID has resolved. Such symptoms may include respiratory problems, myalgia, extreme fatigue, moodiness, cognitive impairment, and difficulty sleeping. Psychological therapies, such as mindfulness, have already demonstrated their effectiveness in pathologies of this type, improving mental health and physical function, as well as reinforcing acceptance and reducing symptoms. Specifically, amygdala-insula training was originally designed for patients with chronic fatigue syndrome as a method of reducing chronic over-sensitization and heightened fear response of the amygdala, which may be behind some of the symptoms related to both with this pathology as with fibromyalgia. A lot of research is currently being done on different types of treatments such as pharmaceutical, biological, dietary, homeopathic and rehabilitation for the treatment of persistent COVID; however, an effective treatment has not yet been found. Therefore, this study aims to evaluate the impact of a retraining intervention of the amygdala and insula for the improvement of the quality of life of patients with persistent COVID.

Conditions

Interventions

TypeNameDescription
BEHAVIORALAIR + MindfulnessAIR + Mindfulness program consists of 8 sessions of 120 minutes/session (10-12 people) Written material and sound recordings will be offered as support elements. The estimated duration of the program is two months.
BEHAVIORALRelaxation conditionRelaxation program consists of 8 sessions of 120 minutes/session (10-12 people) Written material and sound recordings will be offered as support elements. The estimated duration of the program is two months.

Timeline

Start date
2023-09-01
Primary completion
2024-03-31
Completion
2024-03-31
First posted
2023-07-21
Last updated
2025-09-16

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05956405. Inclusion in this directory is not an endorsement.