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Improving Health Status in COVID-19 Long-Hauler

Improving Health Status in COVID-19 Long-Hauler Through an Activity Coaching Programme: a Randomized Control Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06679218
Enrollment
60
Registered
2024-11-07
Start date
2024-11-11
Completion date
2025-01-20
Last updated
2024-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post COVID-19 Condition

Brief summary

This randomized clinical trial investigates the effects of a distance physical activity coaching program on the health of COVID-19 long-hauler. The study evaluates the impact of individualized coaching interventions to improve participants' physical activity and quality of life.

Interventions

OTHERActivity 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.

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.

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients of both sexes. * 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

* Pulmonary, cardiac, neurological, vascular, or orthopaedic pathologies that could limit the execution of the evaluation and intervention. * 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.

Design outcomes

Primary

MeasureTime frame
IPAQ (International Physical Activity Questionnaire)Baseline and at 8 weeks at the end of the intervention
EQ-5D (EuroQol-5 Dimensions)Baseline and at 8 weeks at the end of the intervention
PROMIS (Patient-Reported Outcomes Measurement Information System)Baseline and at 8 weeks at the end of the intervention

Countries

Spain

Contacts

Primary ContactMarie Carmen Valenza, PhD
cvalenza@ugr.es958 248035

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026