Digital Silence and Mental Health

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-25
SponsorAtaturk University

About this trial

Social media use has been linked to negative mental health outcomes, including increased anxiety, depression, stress, poor sleep quality, and difficulties in emotion regulation. Digital detox interventions, which involve reducing or temporarily eliminating digital engagement, have emerged as a strategy to mitigate these effects. However, current evidence regarding their effectiveness is mixed and limited by short-term follow-ups and methodological variability. This study aims to examine the impact of a digital detox intervention on depression, anxiety, stress, sleep quality, and emotion regulation in young adults.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Owning a smartphone

Using social media for ≥ 8 hours per day

Not having a diagnosis related to anxiety, depression, stress, sleep, or emotional regulation

Living in an environment with internet access

Disqualifiers

Having a history of psychiatric diagnosis

Currently using psychiatric medication

Having received psychological counseling in the past 6 months

Having a diagnosis of sleep disorder

Trial design

Design model

Parallel

Treatments tested in this trial

  • digital detox

    Behavioral

    The digital detox intervention differs from other clinical interventions in several key aspects. Unlike pharmacological treatments or traditional psychotherapy, it focuses on behavioral modification by intentionally reducing or eliminating engagement with digital devices and social media for predetermined periods. The intervention emphasizes mindful technology use, limits screen time, and encourages offline activities to restore emotional balance and improve sleep quality. Additionally, it targets the cumulative effects of constant digital exposure, such as information overload, social comparison, and digital dependency, which are not typically addressed in standard mental health interventions. This unique focus on managing digital behavior positions digital detox as a complementary strategy for promoting psychological well-being in young adults.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Control GroupNo intervention 0 interventions
Group B: Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

DASS 21

The DASS-21 was developed by Lovibond and Lovibond as a shortened version of the DASS-42. The psychometric properties of the Turkish version of the Depression Anxiety Stress-21 (DASS-21) scale in both clinical and non-clinical samples were examined by Sarıçam. In the non-clinical sample, the test-retest correlation coefficients were found to be r = 0.68 for the depression subscale, r = 0.66 for the anxiety subscale, and r = 0.61 for the stress subscale. This scale is a 4-point Likert-type instrument consisting of seven items for each of the three dimensions: depression, anxiety, and stress. A score of 5 or above on the depression subscale, 4 or above on the anxiety subscale, and 8 or above on the stress subscale indicates the presence of the respective problem

Time frame
30 day
2

PUKİ

The Pittsburgh Sleep Quality Index (PSQI) was developed by Buysse et al. and its validity and reliability in Turkey were established by Ağargün et al. The scale assesses an individual's sleep quality over the past month and consists of 24 items. Nineteen of these are self-report questions, and 18 items are scored across seven components: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction. Each item is rated on a 0-3 scale, with total scores ranging from 0 to 21. Scores of 5 or below indicate "good sleep quality," while scores above 5 indicate "poor sleep quality." The scale demonstrates a high level of internal consistency with a Cronbach's alpha of 0.80, and its diagnostic sensitivity (89.6%) and specificity (86.5%) are also high.

Time frame
30 day

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ataturk University

Lead sponsor

Agri Ibrahim Cecen University

Sponsor institution

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