Actively Recruiting
Neurocognitive Testing in Long COVID and Postural Tachycardia Syndrome Patients With Normal Saline: A Pilot Study
Led by University of Calgary · Updated on 2026-05-07
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying cognitive dysfunction, often called brain fog, in patients with Postural Orthostatic Tachycardia Syndrome (POTS) and Post-Acute Sequelae of COVID (Long COVID). This study aims to see if a large intravenous infusion of normal saline (999 mL) can improve cognitive function compared to a smaller placebo infusion (50 mL). The study will also measure how these patients perform on cognitive tests compared to healthy controls. Participants will receive either 999 mL or 50 mL of normal saline through an intravenous line in their arm in a crossover design. Each visit includes resting supine with continuous ECG and blood pressure monitoring, standing tests, and cognitive tests such as the Trail-Making Test and Heart Counting Task. The main cognitive assessments use the Cambridge Neuropsychological Test Automated Battery (CANTAB) both seated and standing, with testing sessions lasting up to 90 minutes. After the lab tests, participants complete psychiatric symptom questionnaires online. During each visit, participants undergo continuous monitoring of heart rate and blood pressure during rest, standing, and cognitive testing. Researchers assess cognitive domains like memory, attention, and executive function. The primary outcome is the reaction time on a specific standing task during the procedure. Participants will attend two visits where all tests and infusions are repeated to compare effects. The study includes safety monitoring and uses symptom scores to evaluate participants' responses throughout the sessions.
CONDITIONS
Brief Title
NC Testing in LC & POTS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with Long COVID
- Positive SARS-COV2 test with symptoms lasting more than 12 weeks
- Subjective complaint of brain fog or cognitive dysfunction
- Patients diagnosed with Postural Orthostatic Tachycardia Syndrome (POTS) from Calgary Autonomic Clinic
- Subjective complaint of brain fog or cognitive impairment
- Healthy participants without POTS or brain fog
- Age between 18 and 60 years
- Male or Female
- Able to give informed consent
You will not qualify if you...
- Patients with clear causes for POTS such as dehydration or prolonged bed rest
- Unable to safely stop medicines that affect test interpretation
- Factors preventing protocol completion, including poor compliance or unpredictable schedule
- Unable to give informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 visits each lasting approximately 3 hours, scheduled according to participant convenience
Participants receive intravenous infusions of normal saline in two separate visits to assess cognitive function. Each visit includes IV insertion, infusion of either 999 mL or 50 mL of normal saline, cognitive and neuropsychological testing while seated and standing, and monitoring of blood pressure and symptoms.
2 visits (in-person)
Duration - Approximately 60 minutes after in-lab visits
After the in-lab testing, participants complete a series of validated psychiatric symptom questionnaires online via a secure web application.
Online completion (remote)
Trial Site Locations
Total: 1 location
1
University of Calgary
Calgary, Alberta, Canada, T2N 4Z6
Actively Recruiting
Research Team
S
Satish R Raj, MD MSCI
R
Rasha Hamzeh, RN
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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