The efficacy of mindfulness based stress reduction program on mental well-being and quality of life in patients with COVID-19 after discharge

The efficacy of mindfulness based stress reduction program on mental well-being and quality of life in patients with COVID-19 after discharge: A Randomized Control Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20170218032635N3

Enrollment

100

Registered

2020-12-27

Start date

2021-01-20

Completion date

Unknown

Last updated

2021-01-05

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

Conditions

Condition 1: stress. Condition 2: covid-19. Acute stress reaction Coronavirus infection, unspecified

Interventions

Intervention 1: Intervention group: The intervention in this study is a mindfulness-based stress reduction program that will be a 90-minute mindfulness-based treatment in 8 individual sessions over tw

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age of 18-60 Literacy and the ability to communicate verbally Willingness and ability to participate in mindfulness-based stress reduction virtual sessions Ability to use virtual space and messengers The ability of performing individual daily activities

Exclusion criteria

Exclusion criteria: Changing the patient's health status that prevents his continued participation in the study. Failure to attend meetings and follow up the intervention Changing the patient's condition and re-hospitalization The event of an unintended accident for a person (occurrence of a new physical problem, mental and psychological problem, death of a loved one) that affects the quality of life and well-being of the person.

Design outcomes

Primary

Measure	Time frame
Psychological well being. Timepoint: before intervention and 8 weeks after finishing intervention. Method of measurement: Ryff's psychological well being scale.;Quality of life. Timepoint: before intervention and 8 weeks after finishing intervention. Method of measurement: World Health Organization Quality Of Life- BREF.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfsaneh Sadooghiasl

Tarbiat Modares University

asadooghi@tums.ac.ir+98 21 8288 4875

Outcome results

None listed

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