The effect of motion-based self-care education on quality of life and life expectancy of patients with COVID-19

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150715023216N13

Enrollment

Registered

2022-11-20

Start date

2022-11-22

Completion date

Unknown

Last updated

2023-02-07

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

Conditions

COVID19. Other respiratory disorders

Interventions

Intervention 1: Intervention group: Intervention group: Receiving self-care education motion graphics (in the areas of feeding patients during the recovery period, how to take drugs and drug and nutr

Eligibility

Sex/Gender

All

Age

20 Years to 65 Years

Inclusion criteria

Inclusion criteria: All patients have full consent to participate in the study. Patients only need home quarantine. The patients of the intervention group should have mobile phones with the ability to run motion graphics. Control group patients should have mobile phones with the ability to run PDF. Control group patients should have enough literacy to read and use PDF. Intervention group patients should have good hearing. Patients should be in the age range of 20-65 years. No cancer diseases, no history of organ transplant surgeries and no use of drugs that weaken the immune system.

Exclusion criteria

Exclusion criteria: The people present in the study are not willing to continue cooperating with the research team at any stage of the research and for any reason. Worsening of the disease and requiring hospitalization. Failure to complete or incomplete completion of any of the quality of life and life expectancy questionnaires.

Design outcomes

Primary

Measure	Time frame
The quality of life score from the standard quality of life questionnaire SF-36 in patients with COVID-19. Timepoint: The measurement of quality of life at the beginning of the study (before the intervention) and 14 days after receiving self-care training at home. Method of measurement: Standard questionnaire of quality of life SF-36.;Life expectancy score from Snyder's standard life expectancy questionnaire in patients with COVID-19. Timepoint: The measurement of Life expectancy at the beginning of the study (before the intervention) and 14 days after receiving self-care training at home. Method of measurement: Standard Snyder Life Expectancy Questionnaire.	—

Measure

Time frame

The quality of life score from the standard quality of life questionnaire SF-36 in patients with COVID-19. Timepoint: The measurement of quality of life at the beginning of the study (before the intervention) and 14 days after receiving self-care training at home. Method of measurement: Standard questionnaire of quality of life SF-36.;Life expectancy score from Snyder's standard life expectancy questionnaire in patients with COVID-19. Timepoint: The measurement of Life expectancy at the beginning of the study (before the intervention) and 14 days after receiving self-care training at home. Method of measurement: Standard Snyder Life Expectancy Questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Ghadam

Esfahan University of Medical Sciences

ghadami@nm.mui.ac.ir+98 31 3792 7583

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026