Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
60 participants
INTERVENTIONAL
2024-11-11
2025-01-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Activity Coaching Programme
Activity Coaching Programme
The intervention will consist of individualized physical activity coaching sessions, which will take place twice a week for 8 weeks. These sessions will focus on encouraging progressive and personalized physical activity according to each participant's ability. The sessions will also include relaxation techniques, targeted ventilation and strategies to improve activity management.
Standard medical care and leaflet education
Standard medical care and leaflet education
In addition to standard medical care, patients assigned to this group received a leaflet with information about the main post COVID-19 condition symptoms. This is a control group that was not controlled or monitored by a therapist.
Interventions
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Activity Coaching Programme
The intervention will consist of individualized physical activity coaching sessions, which will take place twice a week for 8 weeks. These sessions will focus on encouraging progressive and personalized physical activity according to each participant's ability. The sessions will also include relaxation techniques, targeted ventilation and strategies to improve activity management.
Standard medical care and leaflet education
In addition to standard medical care, patients assigned to this group received a leaflet with information about the main post COVID-19 condition symptoms. This is a control group that was not controlled or monitored by a therapist.
Eligibility Criteria
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Inclusion Criteria
* Agreed to participate.
* Post COVID-19 condition patients meeting the WHO definition for this disease.
* Sedentary patients according to the cut-off point of the International Physical Activity Questionnaire (IPAQ).
Exclusion Criteria
* Cognitive impairment that prevented them from understanding and answering the questionnaires.
* Patients suffering from a reinfection with SARS-CoV-2.
* Patients with a history of severe or critical COVID-19 disease severity.
* Patients participating in other studies.
18 Years
ALL
No
Sponsors
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Universidad de Granada
OTHER
Responsible Party
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Marie Carmen Valenza
Principal Investigator
Principal Investigators
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Marie Carmen Valenza, PhD
Role: PRINCIPAL_INVESTIGATOR
Universidad de Granada
Locations
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Faculty of Health Sciences. University of Granada
Granada, Granada, Spain
Countries
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Central Contacts
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Facility Contacts
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Marie Carmen Valenza, PT, PhD
Role: backup
Other Identifiers
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DF0102UG
Identifier Type: -
Identifier Source: org_study_id
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