1.
ClinicalTrials.gov; 31/01/2024; TrialID: NCT06247332
Clinical Trial Register
| ICTRP | ID: ictrp-NCT06247332
ABSTRACT
Condition:
Post-acute COVID-19 SyndromeIntervention:
Other: Review of available clinical data sources related to use casesPrimary outcome:
Retrospective SENSING-AI cohortCriteria:
Inclusion Criteria:
- Legal adult
- Diagnosed of long COVID-19 in the last year
- With the presence of any of these symptoms:
- Asthenia (Tiredness)
- Dyspnea
- Shortness of breath
- Anxiety
- Stress
- Depression
- Sleep disorder
Exclusion Criteria:
- Attended to specialized care consultation
- Was admitted in hospital in the last year due to a problem not related to the COVID
complications
2.
ClinicalTrials.gov; 18/11/2022; TrialID: NCT05631171
Clinical Trial Register
| ICTRP | ID: ictrp-NCT05631171
ABSTRACT
Condition:
Post-Acute COVID19 Syndrome;FatigueIntervention:
Behavioral: Adhera® Fatigue Digital ProgramPrimary outcome:
Health-related quality of life;Health-related quality of life;Health-related quality of life;Fatigue;Fatigue;Fatigue;Emotional wellness;Emotional wellness;Emotional wellnessCriteria:
Inclusion Criteria:
- Individuals over 18 years of age.
- With long COVID, according to the World Health Organization (WHO) consensus definition
- Having a history of fatigue symptoms
- Obtain a score between 4 and 10 on the question "By how much do you rate your fatigue
level from 0 to 10 in the last 7 days?", where 0 is no fatigue and 10 is the worst
fatigue imaginable
- Have an Android or iOS smartphone compatible with the intervention program.
- Agree to participate in the study and sign the informed consent form
- Willingness and availability to comply with all study guidelines and procedures
Exclusion Criteria:
- Hospital admission during the period of study participation.
- Participation in another study with pharmacological treatment
- Patients who are not technologically literate or unable to use the mobile application.
- Known severe psychiatric illness or presence of relevant cognitive impairment, at the
discretion of the recruiting physician
- With mobility restrictions that limit the patient's ability to perform mild physical
activity
- Being pregnant
- Patients who do not understand or speak Catalan or Spanish.
3.
ClinicalTrials.gov; 28/07/2022; TrialID: NCT05483829
Clinical Trial Register
| ICTRP | ID: ictrp-NCT05483829
ABSTRACT
Condition:
Post Acute COVID-19 SyndromeIntervention:
Behavioral: Adhera® Fatigue for Long COVID programPrimary outcome:
Behavioral outcome: UsabilityCriteria:
Inclusion Criteria:
- Legal adults (older than 18)
- Long COVID diagnosis within the last year
- In possession of a compatible smartphone (Android OS v4.4 or higher)
- Reporting any of these symptoms:
- Fatigue
- Dyspnea
- Anxiety
- Stress
- Depression
- Sleep disorder
Exclusion Criteria:
- Hospital admission during follow-up due to pathology not related to COVID-19
- Patients without digital literacy or who cannot use the mobile application.
- Known severe psychiatric illness or cognitive impairment
- Being pregnant (or suspected to be pregnant)
4.
ClinicalTrials.gov; 10/01/2022; TrialID: NCT05204615
Clinical Trial Register
| ICTRP | ID: ictrp-NCT05204615
ABSTRACT
Condition:
Post-acute COVID-19 SyndromeIntervention:
Other: Collection of clinical, psychometric and biometric dataPrimary outcome:
Physical Activity Distances;Physical Activity in Steps;Physical Activity Duration;Physical Activity Kcal;Physical Activity Bpm;Physical Activity Heart Rate;Physical Activity Oxygen Saturation;Workouts Kcal;Workouts distances;Workouts Bpm;Workouts Heart Rate;Sleep quality Number of Times Awake;Sleep quality duration;Sleep quality Rapid Eye Movement;Sleep quality Bpm;Sleep quality Breathing;Fatigue Assessment Scale;Dyspnoea Index;Generalized Anxiety Disorder 7-Item Scale;Perceived Stress Scale;Patient Health Questionnaire-9;Oviedo Sleep QuestionnaireCriteria:
Inclusion Criteria:
- Legal adults
- With a long COVID-19 diagnose in the last year
- Reporting any of these symptoms:
- Fatigue
- Dyspnea
- Shortness of breath
- Anxiety
- Stress
- Depression
- Conduct disorder
- Sleep disorder
Exclusion Criteria:
- Hospital admission during follow-up due to pathology not related to COVID-19
- Patients without digital literacy or who cannot use the mobile application.
- Known severe psychiatric illness or cognitive impairment
- Being pregnant (or suspected to be pregnant)
- Discharged after hospital admission due to COVID-19