Long COVID Clinical Trial
Official title:
RECOVER-SLEEP: A Platform Protocol for Evaluation of Interventions for Sleep Disturbances in Post-Acute Sequelae of SARS-CoV-2 Infection (PASC)
The platform protocol is designed to be flexible so that it is suitable for a range of study settings and intervention types. Therefore, the platform protocol provides a general protocol structure that can be shared by multiple interventions and allows comparative analysis across the interventions. For example, objectives, measures, and endpoints are generalized in the platform protocol, but intervention-specific features are detailed in separate appendices. This platform protocol is a prospective, multi-center, multi-arm, randomized controlled platform trial evaluating potential interventions for PASC-mediated sleep disturbances. The hypothesis is that symptoms of sleep and circadian disorders that emerge in patients with PASC can be improved by phenotype-targeted interventions. Specific sleep and circadian disorders addressed in this protocol include sleep-related daytime impairment (referred to as hypersomnia) and complex PASC-related sleep disturbance (reflecting symptoms of insomnia and sleep-wake rhythm disturbance).
Status | Not yet recruiting |
Enrollment | 474 |
Est. completion date | November 2025 |
Est. primary completion date | November 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: • See NCT06404086 for RECOVER-SLEEP: Platform Protocol level inclusion criteria which applies to this appendix Exclusion Criteria: • See NCT06404086 for RECOVER-SLEEP: Platform Protocol level exclusion criteria which applies to this appendix (or sub-study) Additional Appendix A (Hypersomnia) Level Exclusion Criteria: 1. Self-reported sleep duration <6 hours per night 2. Poorly controlled hypertension (systolic blood pressure =140 or diastolic blood pressure =90 mmHg) 3. Moderate to severe hepatic impairment (ie, Child-Pugh class B or C)* 4. Known estimated glomerular filtration rate <30 mL/min/1.73 m2 and/or chronic dialysis* 5. Recent myocardial infarction (<1 year), unstable angina, serious cardiac arrhythmias, or other serious heart problems, at the discretion of the investigator 6. Current use of stimulant or wake-promoting medications, unless a washout is permitted 7. Regular use of prescribed hypnotics for sleep (=3 times per week); washout period is permitted. - characterized by the screening labs: coagulation panel and CMP w/LFTs MODAFINIL EXCLUSION CRITERIA 1. Modafinil can affect drug metabolism given its effect on enzymes such as CYP3A4 and CYP2C19. To assess for drug interactions, investigators should use the Lexicomp Drug Interactions System that is available at most institutions. o If the search yields "D" - Consider Modifying Therapy or "X" - Avoid Combination, then the ACTION is to exclude the potential participant. An important example of this is steroid hormonal contraceptives. - If the search yields "C" - Monitor Therapy, then discuss with site PIs on a case-by-case basis. - If the search yields "A" - No Known Interaction or "B" - No Action Needed, then proceed to screen/include the potential participant. 2. Known severe left ventricular hypertrophy, mitral valve prolapse SOLRIAMFETOL EXCLUSION CRITERIA 1. Concurrent treatment with a monoamine oxidase inhibitor (MAOI) or use of an MAOI within the preceding 14 days 2. Current use of dopaminergic drugs |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Duke University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in total score of the PROMIS 8a SRI to assess sleep-related impairment | The PROMIS 8a SRI form includes a total of 8 items that ask participants to reflect on their sleep-related daytime impairment over the past 7 days with questions rated not at all to very much. T-Scores range from 0 to 100, with a score of 60 being 1 standard deviation above population mean. Higher scores indicate greater sleep-related impairment. | Baseline, End of Intervention (Day 77) | |
Secondary | Change in total score of the PROMIS 8b SD to assess sleep disturbance | The PROMIS 8b SD form includes a total of 8 items that ask participants to reflect on their sleep over the past 7 days with one question rated very poor to very good and the remaining questions rated not at all to very much. T-Scores range from 0 to 100, with > 60 1 SD above population mean. | Baseline, End of Intervention (Day 77) | |
Secondary | Change in PROMIS 10a Fatigue score | The PROMIS 10a Fatigue is a 10-item questionnaire that assesses a participant's fatigue on a scale of 1 (not at all fatigued) to 5 (very much). | Baseline, End of Intervention (Day 77) | |
Secondary | Change in an objective neurocognitive battery score | Baseline, End of Intervention (Day 77) | ||
Secondary | Change in ECog2 measure | Everyday Cognition 2 (ECog2) is a self-report, 41-item questionnaire used to measure measure the participant's perceived capacity to perform activities related to cognitive function, which could impact major activities of daily living and independence. It has been used for patients with mild cognitive impairment, Alzheimer's Disease, and dementia. It takes 5 minutes to complete. | Baseline, End of Intervention (Day 77) | |
Secondary | Change in PASC Symptom Questionnaire responses | Participants will be asked to complete a questionnaire that asks about the presence of PASC symptoms at Baseline and at follow-up visits. This questionnaire includes symptoms that have been associated with PASC. | Baseline, End of Intervention (Day 77) | |
Secondary | Change in total score on the Insomnia Severity Index (ISI) | The ISI is a 7-item, self-report questionnaire that assesses the nature, severity, and impact of insomnia, on a 5-point Likert scale (eg, 0 = not at all, 4 = extremely; scores: from 0 to 28). The ISI asks patients to recall their insomnia symptoms over the past 2 weeks. | Baseline, End of Intervention (Day 77) | |
Secondary | Change in within-person variability (over a 7-day period) in sleep onset time, assessed by sleep diary | Sleep onset time will be assessed by sleep diary | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) nocturnal sleep duration, assessed by sleep diary | Nocturnal sleep duration will be assessed by sleep diary | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) 24-hour sleep duration, assessed by sleep diary | 24-hour sleep duration will be assessed by sleep diary | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) sleep midpoint, assessed by sleep diary | Sleep midpoint is the time half way between start and end of sleep, as assessed by sleep diary | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) nocturnal sleep duration, assessed by activity tracker | Nocturnal sleep duration will be assessed by activity tracker | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) 24-hour sleep duration, assessed by activity tracker | 24-hour sleep duration will be assessed by activity tracker | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) sleep efficiency, assessed by activity tracker | Sleep Efficiency is the percentage of the sleep period spent asleep, as measured by activity tracker | Baseline, End of Intervention (Day 77) | |
Secondary | Change in average (over a 7-day period) sleep midpoint, assessed by activity tracker | Sleep midpoint is the time half way between start and end of sleep, as assessed by sleep diary | Baseline, End of Intervention (Day 77) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05926505 -
Safety and Efficacy of Anakinra Treatment for Patients With Post Acute Covid Syndrome
|
Phase 2/Phase 3 | |
Recruiting |
NCT04872309 -
MUlti-nuclear MR Imaging Investigation of Respiratory Disease-associated CHanges in Lung Physiology
|
||
Completed |
NCT05552612 -
Health-related Quality of Life and Long COVID
|
||
Completed |
NCT05531019 -
COVID-19 Sequelae: Treatment and Monitoring. A Dietary Supplement Based on Sea Urchin Eggs With Echinochroma A
|
N/A | |
Not yet recruiting |
NCT04949386 -
Safety, Tolerability and Efficacy of S-1226 in Post-COVID-19 Subjects With Persistent Respiratory Symptoms.
|
Phase 2 | |
Recruiting |
NCT06118112 -
Living With Long COVID: LONGCOVID-EXPERIENCE
|
||
Completed |
NCT05185674 -
Sociodemographic, Clinical, Quality of Life and Health Care Conditions in COVID-19 Survivors.
|
||
Active, not recruiting |
NCT05965752 -
RECOVER-NEURO: Platform Protocol to Measure the Effects of Cognitive Dysfunction Interventions on Long COVID Symptoms
|
N/A | |
Active, not recruiting |
NCT05965739 -
RECOVER-NEURO: Platform Protocol, Appendix_A to Measure the Effects of BrainHQ, PASC CoRE and tDCS Interventions on Long COVID Symptoms
|
N/A | |
Completed |
NCT05812209 -
Stellate Ganglion Block to Treat Long COVID 19 Case Series
|
||
Recruiting |
NCT05606211 -
Pain in Long COVID-19: The Role of Sleep
|
||
Active, not recruiting |
NCT05713266 -
Using Data From a Multisensor Rapid Health Assessment Device to Predict Decompensation in Long COVID (AIDI)
|
||
Completed |
NCT05679505 -
Vagus Nerve Stimulation for Post-COVID Syndrome
|
N/A | |
Completed |
NCT05601180 -
Evaluation of the Efficacy of Respicure® (Resveratrol / Quercetin) in the Management of Respiratory Conditions Including Asthma,COPD and Long COVID.
|
N/A | |
Not yet recruiting |
NCT06045338 -
Mind Body Intervention for Long COVID
|
N/A | |
Recruiting |
NCT06091358 -
Inspiratory Muscle Training in People With Long COVID-19- A Pilot Investigation.
|
N/A | |
Recruiting |
NCT05566392 -
Longterm Influence of Pediatric Long COVID Syndrome
|
||
Recruiting |
NCT05855369 -
Smell Training and Trigeminal Nerve Stimulation for COVID-related Smell Loss
|
Phase 2/Phase 3 | |
Recruiting |
NCT05572346 -
Digital App for Telerehabilitation in Respiratory Diseases
|
||
Recruiting |
NCT06316843 -
Valacyclovir Plus Celecoxib for Post-Acute Sequelae of SARS-CoV-2
|
Phase 2 |