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The effect of mindfulness counseling on the quality of life of adolescent girls”

“The effect of mindfulness counseling on the health-related quality of life in adolescent girls”

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251114067997N1
Enrollment
106
Registered
2025-12-07
Start date
2026-01-04
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health-Related Quality of Life. Adjustment disorders

Interventions

Intervention 1: Intervention group: In this group, the “Mindfulness Counseling Program” is delivered in 8 weekly group sessions, each lasting 45 minutes. The content of the sessions includes training

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 18 Years

Inclusion criteria

Inclusion criteria: Voluntary participation with informed consent from the adolescent and parents. Female students aged 15–18 years enrolled in high schools. Studying in girls’ high schools in Ahvaz city. Availability during the intervention period (not during exam or vacation time).

Exclusion criteria

Exclusion criteria: Occurrence of a severe stressful event within the past six months, such as the death of a parent or close relative. Presence of diagnosed physical or psychological disorders, based on medical history or clinical evaluation. Use of cigarettes or any addictive substances by the participant. Lack of willingness to participate or continue in mindfulness counseling sessions. Inability to attend the intervention sessions regularly due to illness or family issues

Design outcomes

Primary

MeasureTime frame
The primary outcome variable in this study is Health-Related Quality of Life (HRQoL), which is measured to assess the effect of the 8-session Mindfulness Counseling intervention. Operationally, this variable is defined by the total scores obtained by participants across ten distinct domains of the kidscreen_52 questionnaire. These ten domains, which function as the specific primary outcome measures, include: Physical Health, Psychological Health, Feelings and Mood, Self-Perception, Autonomy, Parental Relationships and Family Life, Social Support and Peers, School Environment, Social Acceptance, and Financial Resources. The intervention’s effect will be determined by comparing the scores across these domains at the pre-test, post-test, and one-month follow-up assessment points. Timepoint: The time points for measuring the primary outcome (HRQoL) are precisely:Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: The standardized Kidscreen-52 Health-Related Quality of Life Questionnaire.

Secondary

MeasureTime frame
The physical health of adolescent girls. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life questionnaire.;Psychological Well-Being. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life questionnaire.item 1-5.;Moods and Emotions. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life questionnaire.item 12-18.;Self-Perception. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life questionnaire.item19-23.;Autonomy. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life questionnaire.item24-28.;Parent Relations and Home Life. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life questionnaire.item29-34.;Social Support and Peers. Timepoint: Before the intervention (Baseline), immediately after the completion of the intervention, and one month after the completion of the intervention. Method of measurement: the standardized Kidscreen-52 health-related quality of life q

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZeinab Sayahi

Ahvaz University of Medical Sciences

zynb72049@gmail.com+98 938 085 0517

Outcome results

None listed

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