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| Name | Class |
|---|---|
| Bangor University | OTHER |
| St George's University Hospitals NHS Foundation Trust | OTHER |
| University of Brighton | OTHER |
| University Hospital Southampton NHS Foundation Trust |
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Cognitive impairment is increasingly recognised as a major component of long Covid, and is estimated to be present in 25-75% of affected individuals. This impairment impacts quality of life and the loss of functional ability has major consequences for affected people, their families and the wider economy given people's difficulty in returning to work.
This study will focus on helping people recover from cognitive Covid. This will involve use of rehabilitation strategies aimed at improving function in those cognitive functions identified in Stage 1 as being most affected, and assessing the benefit of rehabilitation on quality of life and people's ability to return to everyday function. These strategies will be co-produced in collaboration with a group of people living with cognitive Covid. At the end of Stage 2 we will produce a freely available "Covid-19 Cognitive Recovery Guide" for affected people, their close contacts and clinicians.
In conclusion, cognitive impairment is frequently observed in long Covid but at present little is understood about its nature, or how it can be treated. The sheer scale of the CV19 pandemic makes this a top priority unmet need for healthcare worldwide. The aim of this study is to meet this need and to deliver a treatment plan for affected people which will help them return to normal life and working ability.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention | Experimental | cognitive rehabilitation programme. 1h session per week x 10 weeks |
|
| Control | No Intervention | The control group receives treatment as usual, this is, participants will carry on with the care they were receiving prior to entry in the study. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cognitive rehabilitation | Behavioral | Set of restorative and compensatory strategies to rehabilitate cognitive function combined with emotional regulation techniques. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Goal-attainment | performance on goals selected by participants | measured at baseline, 3 and 6 months post-randomisation |
| Measure | Description | Time Frame |
|---|---|---|
| Change in cognitive function | set of tests to measure objective improvements in cognitive function | measured at baseline, 3 and 6 months post-randomisation |
| Change in quality of life (EQ-5D-5L) |
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Inclusion Criteria:
Aged between 30 and 60 years
Evidence of prior CV19 infection:
Cognitive impairment persisting more than three months after the acute CV19 infection, defined in terms of subjective reports of cognitive decline post-infection
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Dennis Chan, Dr | University College, London | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University College London | London | WC1N 3BG | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42384384 | Derived | Vanova M, Patel AMR, Scott I, Gilpin G, Manning EN, Ash C, Wittenberg P, Lim J, Hoare Z, Evans R, Bray N, Kipps CM, Devine C, Ahmed S, Dunne R, Koniotes A, Warren C, Chan D, Suarez-Gonzalez A. Cognitive Rehabilitation and Functional Outcomes in Long COVID-Related Cognitive Impairment: A Randomized Clinical Trial. JAMA Netw Open. 2026 Jul 1;9(7):e2620687. doi: 10.1001/jamanetworkopen.2026.20687. | |
| 39434179 |
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| ID | Term |
|---|---|
| D000094024 | Post-Acute COVID-19 Syndrome |
| D005222 | Mental Fatigue |
| D000086382 | COVID-19 |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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Not provided
| ID | Term |
|---|---|
| D000091942 | Cognitive Training |
| ID | Term |
|---|---|
| D000066530 | Neurological Rehabilitation |
| D012046 | Rehabilitation |
| D000359 | Aftercare |
| D003266 | Continuity of Patient Care |
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| OTHER |
| Greater Manchester Mental Health NHS Foundation Trust | OTHER |
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Measure of quality of life
| measured at baseline, 3 and 6 months post-randomisation |
| Change in Life Space Questionnaire | Measures the extent of mobility | measured at baseline, 3 and 6 months post-randomisation |
| Social Functioning (SF-DEM) | patient reported outcome measure to assess social functioning | measured at baseline, 3 and 6 months post-randomisation |
| Change in Instrumental Activities of Daily Living (IADL) Scale | assessment of independent living skills | measured at baseline, 3 and 6 months post-randomisation |
| Generalised Anxiety Disorder Assessment (GAD-7) | measures levels of anxiety | measured at baseline, 3 and 6 months post-randomisation |
| Change in Patient Health Questionnaire (PHQ-8) | measures depressive disorders | measured at baseline, 3 and 6 months post-randomisation |
| Change in Chalder Fatigue Scale | measures the severity of tiredness in fatiguing illnesses | measured at baseline, 3 and 6 months post-randomisation |
| Change in Pittsburgh Sleep Quality (PSQI) | slef reported questionnaire that assesses sleep quality | measured at baseline, 3 and 6 months post-randomisation |
| Change in DePaul Symptom Questionnaire - Post-Exertional Malaise (DSQ-PEM). | measures presence and severity of post-exertional malaise | measured at baseline, 3 and 6 months post-randomisation |
| Change in Client Service Receipt Inventory (CSRI) | tool used to collect information on the whole range of services and supports study participants may use | measured at baseline, 3 and 6 months post-randomisation |
| Derived |
| Vanova M, Patel AMR, Scott I, Gilpin G, Manning EN, Ash C, Wittenberg P, Lim J, Hoare Z, Evans R, Bray N, Kipps CM, Devine C, Ahmed S, Dunne R, Koniotes A, Warren C, Chan D, Suarez-Gonzalez A. Telehealth-delivered cognitive rehabilitation for people with cognitive impairment as part of the post-COVID syndrome: protocol for a randomised controlled trial as part of the CICERO (Cognitive Impairment in Long COVID: Phenotyping and Rehabilitation) study. Trials. 2024 Oct 22;25(1):704. doi: 10.1186/s13063-024-08554-3. |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D000094025 | Post-Infectious Disorders |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D005221 | Fatigue |
| D012816 | Signs and Symptoms |
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
| D005791 |
| Patient Care |
| D013812 | Therapeutics |
| D006296 | Health Services |
| D005159 | Health Care Facilities Workforce and Services |