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Conscious Awareness Practice in Adolescents

O

Osmaniye Korkut Ata University

Status

Active, not recruiting

Conditions

Risky Behavior

Treatments

Behavioral: Mindfulness

Study type

Interventional

Funder types

Other

Identifiers

NCT06115343
MINDFULNESS PRACTICE

Details and patient eligibility

About

The aim of this study is to reveal the effect of mindfulness on self-efficacy and risky behaviors in adolescents.

Full description

This randomized controlled experimental study was carried out between 18 September and 27 October at Istanbul Bağcılar Necmettin Erbakan Science High School with a total of 60 students (30 experimental group / 30 control group). Research data were collected from the Conscious Awareness-Based Self-Efficacy Scale-Revised (BFÖS-Y), Risky Behaviors Scale (RDS) and Personal Information Form. Ethics committee approval, written institutional permission and written permission from the participants were obtained for the research. In the first week, pre-tests were given to the experimental and control groups, and the experimental group was given 30 minutes of mindfulness training. Mindfulness training continued to be given to the experimental group for the next 5 weeks, and post-tests were given to the experimental and control groups in the last week.

Enrollment

60 patients

Sex

All

Ages

14 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Be between the ages of 14 and 18
  • Agree to participate in the study
  • Being literate and speaking Turkish fluently
  • Have communication and understanding skills

Exclusion criteria

  • Having a physical health problem that may impair group cohesion and integrity

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Experimental Group
Experimental group
Description:
Conscious Awareness application consists of 6 recordings of 30 minutes for 6 weeks.
Treatment:
Behavioral: Mindfulness
Control Group
No Intervention group
Description:
Participants in the control group engage in 6 sessions of 30-minute social activity for 6 weeks.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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