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Effectiveness and Safety of a Tele-Rehabilitation Program on Fatigue and Related Variables in Chronic Fatigue Syndrome and Post COVID Syndrome

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion pushed from Oct 30, 2026 to Dec 30, 2026v5
  2. Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date: Apr 30, 2027 to Oct 30, 2026
    • Study completion date: Sep 30, 2027 to Mar 30, 2027
    • Site details revised
    v4
  3. Primary endpoints: 2 to 1v3 Show 4 more changesShow less
    • Interventions: Conventional exercise (Behavioral), Therapeutic conscious movement (Behavioral) to Conventional exercise (Behavioral), Mindful and conscious movement-based exercise (Behavioral)
    • Secondary endpoints: 8 to 10
    • Study description expanded, about 3 words
    • Study title expanded, about 1 word
  4. Secondary endpoints: details revised at 1 of 8 entries
    • Study description expanded, about 3 words
    • Study title shortened, about 1 word
    v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a randomized, single-blind clinical trial that aims to evaluate the effectiveness of a tele-rehabilitation program based on mindful and conscious movement-based exercise (including adapted yoga, breathing exercises, and body awareness) compared to conventional exercise (low-intensity strength and aerobic training) and usual medical care (control group) over twelve weeks. The study is for people diagnosed with Chronic Fatigue Syndrome/ Myalgic Encephalitis (CFS/ME) or Post-Covid Syndrome (PCS). We will also look at how the program affects the autonomic nervous system by measuring heart rate variability (HRV). All sessions will be delivered remotely via Telehealth, so participants can take part from home. Assessments will be completed online at the beginning of the study, after three months (at the end of the intervention), and again three months later.
Trial Details
NCT Number NCT06978582
Lead Sponsor University of Seville
Conditions
(from sponsor)		 Chronic Fatigue Syndrome/ Myalgic Encephalitis (CFS/ME), Post COVID Syndrome
Related terms Fatigue Syndrome, Chronic, Motor Activity
Enrollment 147 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov