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Effect of educational program based on the theory of reasoned action on sexual risk behaviors in patients with human papillomavirus

Effect of educational program based on the theory of reasoned action on sexual risk behaviors in patients with human papillomavirus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121831453N1
Enrollment
100
Registered
2017-10-08
Start date
2017-02-03
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Human Papilloma Virus. Anogenital (venereal) warts

Interventions

Intervention 1: "The intervention group": designed the training based on the theory of logical action and based on the results of the analysis of the logical action questionnaire as a face-to-face and
Prevention
"Control group": After selecting the intervention and control group and doing the pre-test from both groups, the control group underwent their normal medical treatment, two months after the initial re
"The intervention group": designed the training based on the theory of logical action and based on the results of the analysis of the logical action questionnaire as a face-to-face and face-to-face tr

Sponsors

Vice Chancellor For Research, University of Medical Sciences of Tehran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients with human papillomavirus is based psychiatrists. Minimum age of 18 years. Be literate. Patients have mental and physical disabilities. Willing to participate and cooperate in research. Exclusion criteria from the study: At the same time receive specific training with research from other sources in connection with the behavior Prkhtrjnsy Not wanting to continue to participate in the study for any reason. Acute physical and psychological complications during the treatment process Failure to attend training sessions Lack of complete follow up period

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual Risk Behaviors. Timepoint: Before And Two Months After The Intervention. Method of measurement: Sexual Risk Scale(SRS) With Likert Scale (I Agree, I Think, Disagree).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDR Hooman Shahsavari

Tehran University of Medical Sciences and Health Services

hooman.shahsavari@gmail.com+98 21 6693 7120

Outcome results

None listed

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