Mindfulness Based Intervention on the COVID-19 Related Distress and Mobile Addiction

Impact of Mindfulness Based Intervention on the COVID-19 Related Distress and Mobile Addiction During Pandemic: A Randomized Control Trails

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05415280

Enrollment

Registered

2022-06-13

Start date

2022-08-01

Completion date

2022-12-01

Last updated

2022-06-14

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

Conditions

Psychological Stress

Keywords

psychological stress mobile phone addiction

Brief summary

The interventional study would be conducted to investigate the efficacy of mindfulness based intervention in order to treat psychological stress(anxiety, depression, and stress related COVID-19), and mobile phone addiction during COVID-19 pandemic.

Detailed description

In the current study the data was collected from the young adults (age range 19-35 years). The high scorer from the sample selected from the participants in both control and experimental groups. furthermore, the mindfulness based stress reduction intervention was given to the experimental group. The mindfulness based stress reduction intervention comprised eight weeks period. After the provision of intervention the data for the second phase would be collected.

Interventions

BEHAVIORALMindfulness Based stress reduction

The aim of the psychological intervention to reduce the mental health problems of the participants.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

19 Years to 35 Years

Healthy volunteers

Inclusion criteria

* The participants fulfil the age criteria, students from public and private universities, and provided signed informed consent.

Exclusion criteria

* Participant suffering from chronic physical or psychological disorder. In addition participant who experience death of loved ones during COVID-19 pandemic.

Design outcomes

Primary

Measure	Time frame	Description
COVID-19 related Stress	35 minutes	COVID-19 related stress scale(\<5 minimum, \>72 Maximum)
anxiety and depression	15 minutes	hospitalized anxiety and depression scale (\<7 minimum, \>21 Maximum)

Secondary

Measure	Time frame	Description
mobile phone addiction	35 minutes	smartphone addiction scale (33 minimum, 198maximum)

Countries

Pakistan

Contacts

Primary Contactzia-un nisa

ziaunnisa95@gmail.com03335248819

Outcome results

None listed

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