An interventional study of test group in Social Behavior and Health Behavior, sponsored by Gonabad University of Medical Sciences. Completed at 1 site in Iran, Islamic Republic of. Open to female participants aged 20 Years to 64 Years. Per ClinicalTrials.gov, last updated 2023-06-08.
Sponsored by Gonabad University of Medical Sciences · Not applicable, Interventional, and Supportive care
The goal of this field trial was to compare in emale-headed households. The main question it aims to answer are:
determine the effect of education based on social cognitive theory on the social health of female-headed households in female-headed households in Gonabad.
Women in the intervention group participated in face-to-face and virtual meetings based on social cognitive theory structures for 4 weeks. The control group did not receive any training related to the intervention.
88 studies on the registry are indexed under Social Behavior; 12 are open to participants now.
This study's enrollment of 120 is above the median of 76 across 69 interventional studies indexed under Social Behavior.
Browse Social Behavior studies →Gonabad University of Medical Sciences is the lead sponsor of 7 studies on the registry; none are open to participants now.
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Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Other: test group
Women in the intervention group participated in face-to-face and virtual meetings based on social cognitive theory structures for 4 weeks
social health
Social health is measured by the Keyes Social Health Questionnaire. This questionnaire
Time frame: before
social health
Social health is measured by the Keyes Social Health Questionnaire. This questionnaire includes 20 questions and examines 5 subscales of social prosperity, social solidarity, social cohesion, social acceptance and social participation.relationships with others
Time frame: After 4 weeks
Plan to share: No
No publications or documents are linked to this record.
This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.
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Gonabad University of Medical Sciences