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Acupressure and Qigong in Chronic Fatigue Post COVID-19. (ACUQiG)

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Enrolling

Conditions

COVID-19
Post-COVID-19 Syndrome

Treatments

Other: self- applied acupressure plus Qigong course plus advice literature
Behavioral: advice literature with naturopathy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

International observational studies confirm the high incidence of post-infectious residual syndrome after infection with severe acute respiratory syndrome corona virus 2 (SARS-COV2), which can occur in 10-15% of all infected persons, regardless of the severity of the acute infection. Post corona virus disease 19 (postCOVID-19) patients suffer mostly from symptoms such as fatigue, muscle pain, problems to focus, depression and sleep disturbances.

So far, there are no results of interventional studies for the treatment of chronic fatigue post COVID-19, but there are indicators that post COVID-19 syndrome is a chronic subclinical inflammation, similar to Chronic Fatigue Syndrome / Myalgic Encephalomyelitis CSF/ME, which also often develops from a postviral syndrome. Previously tested and effective strategies for the treatment of chronic fatigue syndrome / myalgic encephalomyelitis (CFS/ME) will be tested in the treatment of chronic fatigue postCOVID-19, in this randomized controlled trial a combination of acupressure and Qigong.

The aim of this project is to evaluate an acupressure treatment plus a Qigong exercise series specifically tailored for chronic fatigue postCOVID-19 , used daily by the patients themselves and regularly supervised, in comparison to the advice literature on the treatment of PostCOVID-19 syndrome alone.

Full description

Prospective two-arm (parallel groups) randomised controlled confirmatory intervention study with mixed methods approach in 2x 100 patients (n=200).

Intervention: self-applied acupressure and online Qigong course over 8 weeks and follow up at week 16.

Group 1: Acupressure + Qigong: Massage of the points daily for 3 minutes per point with the finger or an acupuncture pen (some points can be massaged bilaterally, therefore total approx. 20 min). In addition, twice a week an online guided Qigong course with a duration of 30-45 min. The patients should practise Qigong at least 3 times a week (including the course date). In addition, all patients will receive the guidebook literature for the treatment of complaints after SARS-CoV2 infection.

Group 2: Patients will receive advice literature on the treatment of chronic fatigue after SARS-CoV2 infection. After the end of this study the patients of this group will receive written information and video material regarding the acupressure and Qigong exercises.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. diagnosis of chronic fatigue (after SARS-CoV2 infection)
  2. with at least 3 of 7 criteria at time of study inclusion: sleeping disorder, headaches, joint pain/muscle pain, anxiety/depression, memory impairment/ concentration problems, anosmia, exercise intolerance.
  3. acute SARS-CoV2 infection at least 12 weeks ago
  4. age 18-60 years
  5. visual analogue scale (0-100 mm) physical resilience of maximum 60 mm
  6. SF-36 physical function of maximum 65
  7. technically equipped to participate in the online intervention and willing to follow the study procedure, acupressure and Qigong to perform the exercise series at home
  8. written informed consent available.

Exclusion criteria

  1. fatigue already present before the SARS-CoV2 infection
  2. other underlying diseases leading to symptoms of chronic fatigue, such as major depression, oncological diseases, multiple sclerosis, fibromyalgia and drug abuse
  3. other serious underlying diseases, such as severe pulmonary, cardiac, psychiatric or infectious diseases, which could interfere with study participation or affect the results
  4. ongoing opioid therapy or opioid therapy in the week prior to study entry
  5. chronic use of cannabinoids before or during the study.
  6. start of psychotherapy or interruption of ongoing therapy during study participation
  7. female participants: pregnancy or breastfeeding
  8. participation in another clinical intervention study during study participation
  9. ongoing pension procedure or planned claiming of a pension procedure due to disability
  10. planned inpatient rehabilitation measures during study participation due to PostCOVID-19 -

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

200 participants in 2 patient groups

self- applied acupressure plus Qigong plus advice literature
Experimental group
Description:
daily 20 min of self- applied acupressure over 8 weeks on acupuncture points Yintang, LI4, Pe6, ST36, SP6 and depending on further symptoms plus DU23/24 in hyposmia, LU7 in dyspnoea, GB34 in pain conditions, GB20 in headache OR Anmian in sleeping disorders. The 16 sessions of 45 min Qigong course over 8 weeks will contain live online guided exercises with breathing, stretching and tapping of meridians and exercises such as the crane exercise.
Treatment:
Other: self- applied acupressure plus Qigong course plus advice literature
advice literature
Active Comparator group
Description:
advice literature contains naturopathic remedies such as application of massage-oils, use of herbal teas, meditation techniques, breathing exercises for reconvalescence after COVID19.
Treatment:
Behavioral: advice literature with naturopathy

Trial contacts and locations

1

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Central trial contact

Miriam Ortiz, MD; Joanna Dietzel, MD

Data sourced from clinicaltrials.gov

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