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Tele-coaching in Patients With COVID-19

Effectiveness of Pulmonary Rehabilitation With Tele-coaching in Patients With COVID-19

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04791072
Enrollment
36
Registered
2021-03-10
Start date
2021-03-01
Completion date
2021-03-01
Last updated
2021-03-10

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

Conditions

Covid19, Rehabilitation

Keywords

covid19, rehabilitation, telecoaching

Brief summary

Respiratory exercise training and aerobic exercise training will be given to patients who have been hospitalized in intensive care due to COVID 19 and underwent IMV, who were hospitalized in the service and underwent NIMV or high-flow oxygen inhalation, and whose respiratory symptoms persist after discharge. The patients in the study group will be called by phone once a week and a motivating conversation will be made. No control will be made to the control group. Before and after the training, 6-minute walking test, MRC dyspnea scale, SGRQ quality of life questionnaire and hospital anxiety depression scale will be applied.

Detailed description

Some of the patients with COVID 19 pneumonia still have respiratory symptoms despite being treated. It has been reported that pulmonary rehabilitation programs applied in various models and in a small number to relieve or reduce these symptoms reduce dyspnea, increase exercise capacity and improve quality of life. There is no study reporting the results of a pulmonary rehabilitation program applied to COVID 19 patients in our country. The main purpose of this study is to determine the efficacy of pulmonary rehabilitation applied by telecoach to patients with severe COVID 19 pneumonia or persistent respiratory symptoms. Secondly, it is aimed to present the data of Turkish society to the literature. In accordance with this purpose investigators planed a randomised control clinical study. In our study respiratory exercise training and aerobic exercise training will be given to patients who have been hospitalized in intensive care due to COVID 19 and underwent IMV, who were hospitalized in the service and underwent NIMV or high-flow oxygen inhalation, and whose respiratory symptoms persist after discharge. The patients in the study group will be called by phone once a week and a motivating conversation will be made. No control will be made to the control group. Before and after the training, 6-minute walking test, MRC dyspnea scale, SGRQ quality of life questionnaire and hospital anxiety depression scale will be applied.

Interventions

OTHERExercise

Breathing exercise training Use of incentive spirometry Aerobic exercise training Strengthening exercises

Sponsors

Izmir Katip Celebi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Being treated in intensive care unit due to COVID-19 pneumonia, * Receiving IMV, NIMV, or high-flow oxygen therapy * Patients whose respiratory symptoms persist despite discharge

Exclusion criteria

* Patients with PCR test + * Patients without any complaints. * Patients who are hospitalized and discharged within 10 days * Patients with orthopedic, neurological, cognitive problems

Design outcomes

Primary

MeasureTime frameDescription
Exercise CapacityChange from baseline six minute walk distance at 8 weekSix Minute- walk test

Secondary

MeasureTime frameDescription
Quality of Life AssessmentChange from baseline quality of life at 8 weekSt. George Respiratory Questionnaire; Scores range from 0 to 100, with higher scores indicating more limitations.
Dyspnea AssessmentChange from baseline dyspnea at 8 weekMedical Research Council Scale(MRC); the MRC dyspnea scale is a questionnaire that consists of five statements about perceived breathlessness. (min 1- max 5 point) Higher scores mean a worse outcome.
Anxiety and DepressionChange from baseline anxiety and depression at 8 weekHospital Anxiety and Depression (HAD); The HADS questionnaire has seven items each for depression and anxiety subscales. Scoring for each item ranges from zero to three, with three denoting highest anxiety or depression level. A total subscale score of \>8 points out of a possible 21 denotes considerable symptoms of anxiety or depression.

Outcome results

None listed

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