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Evaluation of the effectiveness of the educational intervention of emotional regulation strategies based on Gross model on emotion regulation strategies and psycho-social burden of women infected with human papillomavirus

Evaluation of the effectiveness of the educational intervention of emotional regulation strategies based on Gross model on emotion regulation strategies and psycho-social burden of women infected with human papillomavirus

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221230056982N1
Enrollment
100
Registered
2023-01-16
Start date
2023-01-26
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Human Papillomavirus. Papillomavirus as the cause of diseases classified to other chapters

Interventions

Intervention 1: Intervention group: After obtaining the written consent, the demographic information questionnaire, the HIP questionnaire and the Gross Emotion Regulation Scale will be completed throu

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Having written informed consent to participate in the study age range of 15-49 years and married The husband knowing that his wife is infected with HPV disease The husband is infected with HPV disease Having Iranian nationality Being a resident of Urmia Having at least fifth grade literacy Definite diagnosis (by a gynecologist) during the last three months with HPV type The absence of malignant diseases Living with husband

Exclusion criteria

Exclusion criteria: Occurrence of pregnancy during the study Unwillingness to cooperate in the continuation of the project Not participating in more than two educational intervention sessions Getting divorced and separated from the husband Not having sex during life Having an acute psychological incident such as losing a family member Having mental illnesses such as severe depression and consuming addictive substances during the study and the last 6 months

Design outcomes

Primary

MeasureTime frame
General psycho-social burden score of women infected with human papillomavirus. Timepoint: Measuring the general psycho-social burden score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Gross's emotional regulation strategies. Timepoint: Measurement of the Gross's emotional regulation strategies score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: Gross's emotion regulation questionnaire.

Secondary

MeasureTime frame
Worries and concerns. Timepoint: Measurement of the Worries and concerns score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Emotional impact. Timepoint: Measurement of the emotional impact score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Sexual impact. Timepoint: Measurement of the sexual impact score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Self image. Timepoint: Measurement of the self image score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Partner and transmission. Timepoint: Measurement of the partner and transmission score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Interactions with doctors. Timepoint: Measurement of the interactions with doctors score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Control/life impact. Timepoint: Measurement of the control/life impact score of infected women at the beginning of the study (before the start of the intervention) and 5 weeks later at the end of the last counseling session and 3 months later. Method of measurement: HIP questionnaire.;Cognitive

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Roghaye Bayrami

Oroumia University of Medical Sciences

Rozabayrami@yahoo.com+98 44 3223 4897

Outcome results

None listed

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