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Investigating the effect of couple-oriented cognitive behavioral therapy based on acceptance and commitment on lifestyle modification in infertile women with poly cystic ovary syndrome

Investigating the effect of couple-oriented cognitive behavioral therapy based on acceptance and commitment on lifestyle modification in infertile women with poly cystic ovary syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240922063120N1
Enrollment
72
Registered
2024-10-25
Start date
2024-11-05
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Condition 1: Life style. Condition 2: Polycystic ovary syndrome. Condition 3: Infertility. Problems related to lifestyle Polycystic ovarian syndrome Female infertility associated with anovulation

Interventions

Intervention 1: Intervention group: After obtaining consent and controlled randomization each of 36 couples in the intervention group, Eligible for initial assessment, will receive 8 sessions of 45 mi

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Having at least reading and writing literacy Couples with primary infertility Women aged 18-40 Suffering from poly cystic ovary syndrome with at least two of the three Rotterdam criteria:1. Oligo menorah . 2. High levels of androgen hormones or symptoms indicating an increase in male hormones such as (hirsutism, acne, etc.) 3. Morphology of poly cystic ovary in the form of 12 follicles (with a diameter of 2 to 9 mm) or ovarian volume greater than 310 cm in at least one ovary with The use of an ultrasound device with a trans vaginal probe >8 MHz is defined Both husband and wife should be willing to attend meetings have a poor lifestyle score of less than 103 or an average of 104-156

Exclusion criteria

Exclusion criteria: Major medical disease (including blood pressure, diabetes with glycosylated hemoglobin [>0.7% HgbA1c)] Mental illness such as depression (according to the participant's statements) Participation in another interventional study Positive pregnancy test Recent adverse events in life Smoking, alcohol and substance abuse (physical and psychological effects) History of participation in lifestyle promotion classes

Design outcomes

Primary

MeasureTime frame
Overall score of health-promoting lifestyle profile. Timepoint: before the start of the intervention, immediately after the completion of 8 weeks of intervention and finally follow-up treatment 2 months after the end of the sessions. Method of measurement: Using the health promoting lifestyle profile questionnaire of Walker et al.

Secondary

MeasureTime frame
BMI ( Body Mass Index). Timepoint: Before the intervention, immediately after the intervention and as a follow-up treatment 2 months after the end of the intervention. Method of measurement: Using the demographic questionnaire used by the researcher.;Menstrual cycle. Timepoint: Before the intervention, immediately after the intervention and as a follow-up treatment 2 months after the end of the intervention. Method of measurement: Using the demographic questionnaire used by the researcher.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Asgari

Ahvaz University of Medical Sciences

nasim.ag2014@gmail.com+98 31 3625 3385

Outcome results

None listed

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