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NCT05422924Completed

A Web-based Platform to Improve Physical Function, Nutrition, and Mindfulness in Patients With Long COVID

A Pilot and Feasibility Study of a Web-based Platform to Improve Physical Function, Nutrition, and Mindfulness in Patients With Long COVID

Source: ClinicalTrials.gov · Last updated 6 Mar 2025

Brief summary (registry, in English)

Patients with COVID-19 may experience prolonged physical and psychological symptoms after weeks or months of the infection. This may be caused by a combination of factors including poor nutrition, low physical activity, and lack of emotional support. Leading to poor overall health and low quality of life. This evidence indicated that people with long COVID-19 need a personalized intervention. Our objective is to determine if the use of an online application that is based on preventive self-care and that includes nutrition and mindfulness will be feasible to use for patients with long COVID.

Status (registry)
Completed
Study type
Interventional
Enrollment
45 (actual)
First submitted
16 Jun 2022
Start date
25 Aug 2023
Primary completion date
31 Oct 2023
Lead sponsor
University of Alberta
NCT number
NCT05422924

What you commit to

  • Study type: Interventional
  • Participants enrolled: 45
  • From 25 Aug 2023 to the primary completion date, 31 Oct 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with severe mobility impairment (People without sufficiently mobile to come to the study centre).
  • Diagnosis of severe mental health disorders (e.g., depression, anxiety, eating disorders).
  • Major visual or hearing impairment or other serious illness that would preclude participation.

Other

  • Individuals with pacemakers or other internal electrical medical devices.
  • Suffer from claustrophobia.
  • Pregnancy or lactation.
  • No internet access.
  • Not able to understand and communicate in English.
  • Living in assisted living situations or a nursing home.
  • Individuals who fell more than 3 times in the last month. Because of the risk of doing a physical activity unsupervised.
  • Not willing to make a change in their lifestyle (Readiness to change).

Who the study is looking for

  • Aged ≥ 18 years.
  • COVID diagnosed (PCR positivity) \>12 weeks at time of screening and have persistent symptoms.
  • Body mass index (BMI) \>18.5kg/m2 and \< 35 kg/m2.
  • People with long COVID syndrome diagnosis enrolled in the Kaye Edmonton Clinic.
  • Have mild to moderate long COVID syndrome (Based on the Post COVID-19 Functional Status Scale from 0-3).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alberta
Coordinator of this site? Confirm its status
EdmontonCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.