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Evaluation of the effects of adolescent health promotion training package on treatment of poly cystic ovary disease

Evaluation of the effects of adolescent health promotion training package on treatment of poly cystic ovary syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200114046123N1
Enrollment
120
Registered
2020-01-23
Start date
2020-09-22
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

poly cystic ovarian syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: "Intervention group:" Face-to-face teaching polycystic ovary syndrome adolescents are conducted in eight 45-minute sessions of lecture, question and answer provided by the researcher.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
14 Years to 18 Years

Inclusion criteria

Inclusion criteria: Written parental and student agreement Girls ages 14 to 18 who are single and without sexual relation At least 2 years passed from the juvenile menarche According to ASRM criteria, 2 items of PCOS symptoms were diagnosed Be healthy in terms of all diseases including liver, kidney, thyroid, heart and skeletal diseases Have not taken any female hormone or metformin medication for at least three months before entering the study Have no smoking at least three months before the intervention Do not use drugs or alcohol Not have severe mental illness (which requires medication) Do not exercise professionally or attend school sports team Do not follow a specific diet

Exclusion criteria

Exclusion criteria: Adolescents who failed to perform 1/3 of the recommended physical activities per month for any reason Adolescents who for any reason failed to attend 1/3 of the classes held at the school. Adolescents who have not completed any form of physical activity and diet assessment for at least one month for any reason. Adolescents who affected by a specific illness or need to take a particular drug after entering the plan. Adolescents who they or their parents are reluctant to continue in the project for any reason.

Design outcomes

Primary

MeasureTime frame
Life style modification in adolescent with poly cystic ovarian syndrome. Timepoint: before intervention, 6 and 12 after intervention. Method of measurement: diet and physical activity questionnaire.;Menstrual cycleregularity,. Timepoint: Before intervention and 6, 12 months after intervention. Method of measurement: Menstrual cycles are 15 indicates moderate or severe Hirsutism.;Anthropometric index. Timepoint: Before intervention and 6, 12 months after intervention. Method of measurement: weight,height, waist, and hip circumstance.

Secondary

MeasureTime frame
Blood bio markers. Timepoint: before intervention and after 12 months. Method of measurement: Blood test.;Sonography Items. Timepoint: before intervention and after 12 months. Method of measurement: Transabdominal Sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Abdolahian

Shahid Beheshti University of Medical Sciences

abdolahian.s@sbmu.ac.ir+98 21 8820 2512

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026