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Column | Value |
---|---|
Trial registration number | NCT05298878 |
Full text link
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
|
First author
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
|
Contact
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
tania.janaudis-ferreira@mcgill.ca |
Registration date
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
2022-03-28 |
Recruitment status
Last imported at : Sept. 9, 2022, midnight Source : ClinicalTrials.gov |
Recruiting |
Study design
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
RCT |
Allocation
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Randomized |
Design
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Parallel |
Masking
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Blind label |
Center
Last imported at : March 15, 2023, 4 a.m. Source : ClinicalTrials.gov |
multi-center |
Study aim
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Long covid |
Inclusion criteria
Last imported at : Nov. 9, 2022, 4 p.m. Source : ClinicalTrials.gov |
inclusion criteria: (i) adult patients (18+ years old) who have had a confirmed or probable covid-19 infection and who have self-reported persisting symptoms of either reduced mobility, muscle weakness, dyspnea, or fatigue; (ii) participants must be technologically capable of connecting (either independently or through household members) with an online videoconferencing platform through an e-mail invitation; and (iii) be able to collaborate with the research assistant to complete the virtual assessment sessions or have a family member available to help. |
Exclusion criteria
Last imported at : April 7, 2022, 9:30 p.m. Source : ClinicalTrials.gov |
(i) pre-existing or newly identified severe cognitive impairment; (ii) inability to speak or comprehend english or french; (iii) known or self-reported acute and/or uncontrolled cardiac, musculoskeletal, or neurological condition that might render rehabilitation participation unsafe. |
Number of arms
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
2 |
Funding
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
McGill University Health Centre/Research Institute of the McGill University Health Centre |
Inclusion age min
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
18 |
Inclusion age max
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
100 |
Countries
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Canada |
Type of patients
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Patients recovered from covid |
Severity scale
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
N/A |
Total sample size
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
132 |
primary outcome
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Change in the basic mobility domain of the Activity Measure for Post-Acute Care (AM-PAC) |
Notes
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
None |
Phase
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
Not reported |
Arms
Last imported at : March 29, 2022, 2:30 p.m. Source : ClinicalTrials.gov |
[{"arm_notes": "nan", "treatment_id": 584, "treatment_name": "Home-based virtual rehabililtation", "treatment_type": "Rehabilitation", "pharmacological_treatment": "Non pharmacological treatment"}, {"arm_notes": "nan", "treatment_id": 2188, "treatment_name": "Standard of care", "treatment_type": "Standard of care", "pharmacological_treatment": "Standard of care"}] |