Cysteine-rich Whey Protein for Post COVID-19 Cognitive Impairment
Intervention with Consolidated Cysteine (Immunocal) 20 g per day
+ Cognitive rehabilitation workshops
COVID-19+19
+ Behavior
+ Mental Disorders
Treatment Study
Summary
Study start date: July 1, 2024
Actual date on which the first participant was enrolled.This study focuses on finding ways to help people who have recovered from COVID-19 but are now facing issues with memory and thinking, known as cognitive impairment. The trial takes place in Cali, Colombia, and involves adults who have mild to moderate difficulties with cognition after COVID-19 but did not previously use the supplement Immunocal. By testing the effects of a cysteine-rich whey protein isolate called Immunocal, along with a structured neuropsychological rehabilitation program, the research aims to improve cognitive functioning in these individuals. This study is important because it could offer new therapies to help individuals regain their cognitive health after COVID-19. Participants in this study are divided into three groups: one receiving Immunocal supplementation, another undergoing neuropsychological rehabilitation, and a control group receiving no treatment. Immunocal is taken daily for 12 weeks by mixing and consuming the supplement. The effectiveness of these interventions is measured through cognitive tests that evaluate attention, memory, and other mental functions, as well as a physical test assessing lower body strength and endurance. These assessments help determine how well the interventions work in improving cognitive and physical health. Participants' symptoms and overall health are also monitored by doctors throughout the study to ensure safety and gather comprehensive health data.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.120 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion: * Adults ≥18 years with confirmed prior COVID-19 * with persistent cognitive symptoms * able to complete testing * and willing to consent. Exclusion: * Pre-existing dementia or major psychiatric illness * whey protein allergy - participation in another cognitive trial * severe hepatic/renal/metabolic disease, pregnancy * or any condition interfering with participation.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location