The effects of an information provision intervention about menstruation aimed at male adolescents: a cohort-nested randomized controlled trial in Uganda as a part of Research Network for Design and Evaluation of Adolescent Health Interventions and Policies in Sub-Saharan Africa (DASH)
- Conditions
- Menstrual health
- Registration Number
- DRKS00034169
- Lead Sponsor
- Heidelberg Institute of Global Health (HIGH)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Male
- Target Recruitment
- 666
The following inclusion criteria are those for the overall DASH cohort, with the addition of restricting the RCT to male participants between ages 10 and 19 years:
? Study participant is between ages 10 and 19 years;
? Study participant is male;
? Minors (i.e. less than 18 years of age): the parents or guardians provide written informed consent, and the minor participant provides informed assent;
? Adults (i.e. 18 years of age and above): provides written informed consent; and,
? Study participant is a resident of the study area and intends to stay in the study area for the duration of the study.
The following exclusion criteria are those for the overall DASH cohort:
? Participants who do not meet the above-listed criteria will be excluded;
? Participants with chronic illnesses will be excluded since it may hinder their autonomy;
? Participants whose capacity to make meaningful decisions is in question because they are cognitively impaired”;
? Individuals with communication difficulties.
The only additional criteria applied specifically for this randomized trial is that the participant will be excluded from analysis if he does not respond to the questions that are used to generate the outcome measures.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Survey items:<br>Interest in learning about menstruation (cross-sectionally at a later point in the survey, and again 1 year after intervention is provided, when the next wave of the survey is administered);<br>Self-reported teasing behavior regarding menstruation (cross-sectionally at a later point in the survey, and again 1 year after intervention is provided, when the next wave of the survey is administered).
- Secondary Outcome Measures
Name Time Method Survey items:<br>Knowledge about the menstrual cycle (cross-sectionally at an earlier point in the survey, and again 1 year after intervention is provided, when the next wave of the survey is administered);<br>Knowledge about fertility in the menstrual cycle (Cross-sectionally at an earlier point in the survey, and again 1 year after intervention is provided, when the next wave of the survey is administered);<br>Discomfort with the topic of menstruation (cross-sectionally at a later point in the survey, and again 1 year after intervention is provided, when the next wave of the survey is administered);<br>Perceived normality of menstruation (cross-sectionally at a later point in the survey, and again 1 year after intervention is provided, when the next wave of the survey is administered).