Feasibility Study of Adhera® Fatigue Digital Program for Patients With Long COVID-related Fatigue

ABSTRACT

ConditionPost-Acute COVID19 Syndrome;Fatigue

InterventionBehavioral Adhera® Fatigue Digital Program

Primary outcome:Health-related quality of life;Health-related quality of life;Health-related quality of life;Fatigue;Fatigue;Fatigue;Emotional wellness;Emotional wellness;Emotional wellness

Criteria
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.