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Quality of Life After Hyperbaric Oxygen Therapy in Post-COVID Patients

Quality of Life After Hyperbaric Oxygen Therapy in Post-COVID Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06159309
Acronym
QoL COVID HBOT
Enrollment
200
Registered
2023-12-06
Start date
2023-02-06
Completion date
2025-08-31
Last updated
2025-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Long COVID, Long Covid19, Long Covid 19, Long COVID-19 Syndrome

Keywords

registry, covid, long-covid, post-covid

Brief summary

Post-Covid syndrome, also known as long Covid, is a clinical condition in which patients experience long term symptoms after Covid-19 infection. Treatment options for post-Covid are not effective. Therefore, there is an urgent need for a novel therapy. The first study results of HBOT in post-Covid patients are promising. Previous research from Israel has shown improvements in quality of life after HBOT. However, long term results are unknown. Therefore, this study aims to evaluate quality of life at one year after hyperbaric oxygen therapy in post-Covid patients with cognitive symptoms. It is hypothesized that quality of life at one year after HBOT is improved. Furthermore, this study aims to evaluate return to work after HBOT. To our knowledge this was not done before. An observational prospective cohort study will be conducted to answer the research questions. All post-Covid patients who are treated with hyperbaric oxygen therapy in participating centers, will be eligible for inclusion. Questionnaires and medical doctor consultations will be used in order to collect all data. There are no risks for participants, since only 7 questionnaires are not part of standard clinical care. The burden is approximately 40 minutes extra in total for participants, compared to standard clinical care.

Detailed description

The study design is a prospective observational cohort study. Questionnaires and medical doctor consultations will be used in order to collect all data. All patients treated with HBOT have medical doctor consultations at baseline and every 10th session of HBOT (standard clinical care). At baseline, the following characteristics will be collected: gender, age, BMI, medical history, Covid infection information, vaccination status, work status before Covid infection, previous Covid treatments, hospital and/or intensive care unit admission during Covid infection and smoking status. Furthermore, all patients treated are asked to fill out the SF-36 and EQ-5D questionnaires, a proprietary post-Covid symptoms questionnaire, and a questionnaire regaring work status. These questionnaires are repeated after 20, 40 (50) sessions of HBOT and after 3 and 12 months after the last treatment session. During the following medical doctor consultations, side effects, changes in medication and interruptions of HBOT will be recorded as well to monitor compliance. An interim analysis will be performed after 6 months to continue or stop treatments, based on the clinical results (as measured with the Physical Component Score of the SF-36 questionnaire). The minimal clinically important difference (MCID) to warrant early termination of therapy is if \<5% of patients improves 3 points. The upper limit (and reason to continue) is if \>50% achieve an MCID of 7 points.

Interventions

OTHERHyperbaric oxygen therapy

HBOT per local protocol, i.e. 40 sessions 2.4 ATA, at the discretion of the hyperbaric physician

Sponsors

Rutger Lalieu
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Long COVID patients who are reffered for treatment with hyperbaric oxygen therapy * Patients are suffering from cognitive symptoms for >3 months after Covid infection

Exclusion criteria

* Patients who are not able to fill in questionnaires and informed consent. * Patients who can't read or do not understand the Dutch language

Design outcomes

Primary

MeasureTime frameDescription
Quality of life 3 and 12 months3 and 12 monthsIs the expected improvement in quality of life in Long COVID patients after treatment with HBOT maintained at 12-months follow-up

Secondary

MeasureTime frameDescription
Long Covid symptoms3 and 12 monthsWhat symptoms do Long COVID patients who were referred for HBOT suffer from?
Cognitive complaints3 and 12 monthsIs there any improvement of symptoms in Long COVID patients with cognitive symptoms during HBOT and after HBOT?
Work3 and 12 monthsDo changes in absence at work occur after treatment with HBOT in Long COVID patients with cognitive symptoms?
Risk factors quality of life3 and 12 monthsWhat are risk factors for low health related quality of life in Long COVID patients with cognitive symptoms who are treated with HBOT?
Profile of non-responders versus responders3 and 12 monthsWhat are the differences in baseline characteristics of patients that are non-responders and responders after HBOT?

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026