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IRCT20160808029255N12 IRCT 2021-12-23 Shahroud University of Medical Sciences The effects of the psycho-sexual intervention on help-seeking in coping with sexual concerns of young women The effects of the psycho-sexual intervention on help-seeking in coping with sexual concerns of young women, a randomized controlled trial 2022-01-05 anticipated 140 Complete https://irct.ir/trial/60525 interventional Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: In this study, the randomization method will be randomized block design with a block size of 4. The block randomization method is designed to randomize participants into groups that result in equal sample sizes. This method is used to ensure a balance in sample size across groups over time. in this clinical trial with control and treatment groups, a randomized block procedure would be as follows: (1) block size of 4 will be chosen, (2) possible balanced combinations with 2 A (intervention) and 2 B (control) subjects will be calculated as 6 (BBAA, BABA, BAAB, ABBA, ABAB, AABB) and (3) blocks will be randomly chosen to determine the assignment of all participants. N/A Condition 1: Help-seeking. Condition 2: Help-seeking intention. Condition 3: Openness to help-seeking. Condition 4: Self-stigma. Condition 5: Sexual assertiveness. Intervention 1: The intervention group will have access to the content of the intervention as a mobile application weekly for 6 weeks, and during this time, in peer's WhatsApp group, the content of the intervention will be analyzed weekly by the researcher for further training and the asked questions of individuals will be solved in the group. We will ask them to share content with their husband standard questionnaires will be completed before and immediately after intervention and 2 months after the intervention. Intervention 2: The control group will receive the mobile application but they did not access the intervention content until the end of the research. Then, based on the ethics of the research and their willingness can use the content of Intervention. Standard questionnaires will be completed before, immediately after 6 sessions of intervention, and 2 months after the intervention in the control group. Yes - There is a plan to make this available What will be shared: Data of the study would be available after the unrecognizable process of participants. When: Six months after publications of findings To whom: Data of this research would be available for academic researchers Conditions: Data of this study would be available for the same research Where to obtain: Dr. Raziyeh Maasoumi- email: r_masoumi@sina.tums.ac.ir How to obtain: Initial correspondence by email, on-site visit, and presentation of a proposal similar to the present study, provide sufficient evidence for the similarity of its research to the present study, study proposal by the present investigator, decision making and announcement of the result by the investigator to the researcher for access to data Providing the data file for use locally Comments:
public Raziyeh Maasoumi
East Nosrat, Towhid Sq.
Tehran Iran (Islamic Republic of) 1419733171 +98 21 6105 4214 r_masoumi@sina.tums.ac.ir Tehran University of Medical Sciences scientific Raziyeh Maasoumi
East Nosrat, Towhid Sq.
Tehran Iran (Islamic Republic of) 1419733171 +98 21 6105 4214 r_masoumi@sina.tums.ac.ir Tehran University of Medical Sciences Iran (Islamic Republic of) Reading and writing literacy Urbanization Marriage No pregnancy history Sexuality active At least one year of living together Not being pregnant and menopause Having a mobile phone with Android system Internet access 18 years 40 years Female Unwillingness of the women to continue participating in the study N/A N/A The intervention group will have access to the content of the intervention as a mobile application weekly for 6 weeks, and during this time, in peer's WhatsApp group, the content of the intervention will be analyzed weekly by the researcher for further training and the asked questions of individuals will be solved in the group. We will ask them to share content with their husband standard questionnaires will be completed before and immediately after intervention and 2 months after the intervention. The control group will receive the mobile application but they did not access the intervention content until the end of the research. Then, based on the ethics of the research and their willingness can use the content of Intervention. Standard questionnaires will be completed before, immediately after 6 sessions of intervention, and 2 months after the intervention in the control group. Help-seeking. Timepoint: Before the intervention, immediately and 2 months after the intervention. Method of measurement: Actual help-seeking questionnaire. Help-seeking intention. Timepoint: Before the intervention, immediately and 2 months after the intervention. Method of measurement: General help-seeking questionnaire. Openness to help-seeking. Timepoint: Before the intervention, immediately and 2 months after the intervention. Method of measurement: Modified version of attitudes toward professional help-seeking scale. Self-stigma. Timepoint: Before the intervention, immediately and 2 months after the intervention. Method of measurement: Self-stigma questionnaire. Sexual assertiveness. Timepoint: Before the intervention, immediately and 2 months after the intervention. Method of measurement: Hulbert sexual assertiveness questionnaire. Shahroud University of Medical Sciences Approved 2019-11-12 Ethics committee of Shahroud University of Medical Sciences Shahroud University of Medical Sciences and Health Services, Hafte Tir Square, Shahroud, Iran. Shahroud Semnan Iran (Islamic Republic of)