An interventional study of tele lactation and face to face in Breast Feeding, Primipara Women and the Study Focus on Health Education for Primipara, sponsored by Assiut University. Completed at 1 site in Egypt. Open to female participants. Per ClinicalTrials.gov, last updated 2026-11-03.
Sponsored by Assiut University · Not applicable, Interventional, and Prevention
Among 14 studies in Breast Feeding with a site in Egypt — 4 open to participants now, 4 under way, none of them phase 3. Breast Feeding · Egypt.
Among the 14 studies in Breast Feeding with a site in Egypt, this one is the 5th largest by enrollment of the 12 interventional ones, is one of 5 that started in 2025, is one of 12 with no phase, and was the 14th registered.
1,081 studies on the registry are indexed under Breast Feeding; 217 are open to participants now.
This study's enrollment of 132 is above the median of 100 across 844 interventional studies indexed under Breast Feeding.
Browse Breast Feeding studies →4 of the 14 studies in Breast Feeding with a site in Egypt are open now, in 1 country. Each count lists the studies.
Of the 126 Breast Feeding studies recruiting now, 66 (52%) set no upper age limit and 58 (46%) stop at 75 or younger; 54 take children under 18; 76 take healthy volunteers.
This study: female · no healthy volunteers.
The full table on the hub →14 studies; the count open now beside each. This study's row is marked.
First in 2003; this study’s year is marked. 5 started in 2025.
Median enrollment 87 across the 12 interventional studies, 170 across the 2 observational. Of the 9 that completed or were terminated, 0 (0%) have results posted.
None of the 14 has an industry lead sponsor. The 7 most frequent:
Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.
Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Assiut University has 8 studies filed under Breast Feeding — fewer than ten, so there is no comparison to draw.
None of the studies under way reaches primary completion within a year.
Among the 14 studies in Breast Feeding with a site in Egypt, from their registry updates:
This study aims to evaluate and compare the effectiveness of a face-to-face intervention program and a tele-lactation intervention program on breastfeeding myths, knowledge, self-efficacy, and practices among primiparous mothers. Participants will be assigned to receive either face-to-face or tele-lactation guidance and support. Breastfeeding knowledge, self-efficacy, and practices will be assessed to determine the impact of each approach on improving outcomes for first-time mothers
Inclusion 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.
provide health education about breastfeeding to women via whatsapp
Behavioral: tele lactation
provide health education about breastfeeding to women via face to face
Behavioral: face to face
routine care
provide health education about breastfeeding to women via whatsapp
provide health education about breastfeeding to women via face to face
breastfeeding knowledge
The total knowledge score will be organized as follows: poor knowledge, if the total response score ˂ 50 %, neutral knowledge if the scores range from 50% to 75%, and good knowledge if the scores are\>75%
Time frame: 2 months
Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF)
Assessed using the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF), which consists of 14 items rated on a 3-point Likert scale (1 = not confident to 3 = confident). Total scores range from 14 to 42, with higher scores indicating better breastfeeding self-efficacy
Time frame: 2 months
primipara reported practices
This tool consists of 28 items divided into four sections:preparation for breastfeeding (6 items), practices for latch on (7 items), practices during feeding (8 items), and post-feeding practices (7 items) Scoring system The total breastfeeding practice score ranged from 0 to 28. One point was awarded for each practiced item, and zero points were given for each item not practiced. A total score was calculated as a continuous variable and presented as the mean and standard deviation, with a higher mean score indicating a higher level of breastfeeding practice
Time frame: 2 months
Breastfeeding-related taboos and myths among Primiparous Women
This 22-item tool assessed breastfeeding myths using factual and myth-based statements scored on a 2-point scale (1 = incorrect, 2 = correct), with reverse scoring applied to myths Total scores ranged from 22 to 44, where higher scores indicated better knowledge and fewer misconceptions
Time frame: 2 months
Ran from Oct 2025 to primary completion in Oct 2026, 12 months.
Of 502 non-industry interventional studies with no phase under Breast Feeding, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 23. This study's 12 months is close to that.
Counting every sponsor, half of 510 studies reached it within 12 months; a quarter within 6 and three quarters within 23.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.
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