CClinicalTrials.gg
CompletedNCT03308058Updated Sep 28, 2023Results posted

Feasibility of a Touch Screen Computer Based Breast-feeding Educational Support Program

An interventional study of Breastfeeding computer education in Pregnancy Related, sponsored by University of Nebraska. Completed at 1 site in United States. Open to female participants aged 15 Years to 35 Years. Per ClinicalTrials.gov, last updated 2023-09-28.

Sponsored by University of Nebraska · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
15 Years to 35 Years
Sex
Female
01

Study summary

Breastfeeding has many positive and long lasting impacts on the health of infants and mothers. The investigators propose to develop a bilingual touch screen computer based breastfeeding educational support program to promote breastfeeding among Hispanic rural women living in Scottsbluff area of rural Nebraska. An interactive, tailored, touch screen, bilingual breastfeeding educational program will be developed to deliver breastfeeding education to enhance partial or exclusive breastfeeding. An experimental two-group repeated measures design will be utilized. Ninety four prenatal Hispanic rural women aged 15 years and above will be enrolled and randomly assigned to either the intervention (computer based program, N=47) or attention control (printed educational material, N=47) groups at the Regional West Medical Center in Scottsbluff. Information gathered will include socio-demographics, familiarity with use of technology and health literacy assessment. Process variables measured will include breast-feeding knowledge and breast-feeding self-efficacy. Primary and secondary outcomes include breast-feeding duration in binary categories (partial or exclusive) and number of sick baby medical visits and months of illnesses. All assessments will be done at baseline, days 3 and 7, weeks 2 and 6 and months 3 and 6 in both the intervention and attention intervention groups. The current proposed study may help advance our understanding to use health information technology as a medium to disseminate bilingual health education programs in rural settings. This exploratory study will lay a foundation for a larger multicenter randomized controlled clinical trial to evaluate the impact of computer based educational intervention to promote sustainability of breastfeeding among women across diverse settings.

Read the detailed description

Two separate focus groups one in English and Spanish will be performed with six Hispanic rural women with history of previous pregnancy will be enrolled at the Regional West Medical Center (RWMC), Scottsbluff, NE. The focus group of 2 hours duration will be performed at the antenatal clinic at RWMC during months 2 and 3 of the study. The focus group will help examine factors that affect the decision to continue breast-feeding in pregnant Hispanic rural women and will guide development of bilingual (English and Spanish) breast-feeding educational modules during months 4 and 5 of the study. Dr. Aguirre and Ms. Salazar will be responsible for subject recruitment, focus group assessments and would act as a moderator and respond to questions and comments during the focus groups. The focus group interviews, analysis and development of breast-feeding educational modules in English and Spanish will be finalized during the first 5 months of the study. The focus group sessions will be audio recorded and stored in a locked cabinet. The sessions recordings will be destroyed at the end of the research study.

Computer-based Breast-Feeding Educational Support Program: The investigators will modify existing touch screen, computer based interactive Patient Education and Motivation Tool (PEMT) to deliver bilingual, breast-feeding educational support program. The existing PEMT platform allows users to dynamically change the educational content either to English or Spanish. The modification of the existing PEMT will occur during months 5-7 and will include several stages:

(i) PEMT modification design (ii) Tailoring (iii) Expert Pretesting using Heuristic evaluation (iv) Usability and User Testing

Intervention and Evaluation:

The subjects will be randomly enrolled using a 1:1 method with every other subject enrolled randomized to either the control or intervention group, at RWMC, Scottsbluff. Eligible individuals, who will meet the inclusion criteria, will be assigned into either intervention (bilingual Computer based Breast-feeding Educational Support program) or attention control (bilingual breast-feeding printed educational material) groups using a computer generated random id during the subject's prenatal visit (i.e. anytime during last six weeks of their pregnancy). Once randomized, baseline information will be gathered in both the groups.

The difference between the two study groups is that subjects in the intervention (bilingual Computer based Breast-feeding Educational Support program) will record their baseline assessment on a computer and receive tailored breast-feeding education compared to the attention control (bilingual printed breast-feeding educational materials) who will record their baseline information on paper and receive printed breast-feeding educational material. Using self-reported responses of the individuals in the intervention group (bilingual computer based breast-feeding educational support program), the decision logic and algorithm will process the information and deliver tailored breast-feeding educational messages in varied multimedia formats using a combination of text, images, and animations to account for the literacy levels of the subjects.

Appropriate feedback will be given in the form of reinforced educational messages and encouragement and motivational prompts for those using the computer based program. Educational session in both the groups will last for 30 minutes. The first educational session will be performed during the postpartum period, one day before the discharge from the hospital followed by week 6, months 3 and 6. Specific individualized interventions, especially during the initial critical 2-6 week period, are needed to prevent deterioration in intention levels for breast-feeding for 6 months and breast-feeding self-efficacy levels within the first 2 weeks postpartum which could lead to the decision to discontinue breast-feeding. Subjects in both the groups will be given telephone reminders for follow up educational sessions. The touch screen computer based Breast-feeding Educational Support program will be placed on a mobile cart in the outpatient clinic of the RWMC, Scottsbluff for the duration of the study and will be collected after the completion of the research.

There will be no repercussions to subjects since the touch screen computers will be placed at the RWMC and will be used by the subjects enrolled in the study at this site. A web based version will also be available for an ongoing support to subjects in the intervention group. A research assistant will be available to guide the subjects in both the intervention (during the use of the tablet pc program) and the control groups (printed educational material) if needed. The breast-feeding educational modules and data collection instruments will be both in English and Spanish.

02

Conditions studied

  • Pregnancy Related

Keywords

  • Breastfeeding Rural Hispanic Pregnant
03

Who can participate

Ages eligible
15 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Hispanic females age 15 years and above
  • Pregnant
  • Agreeing to participate in the study
  • Understand spoken English
  • Telephone at home
  • Available for follow-up interview.

Exclusion criteria

Exclusion Criteria:

  • mental and physical challenge that makes it difficult to use the touch based computer program
  • unavailability for telephone follow-up and
  • involvement in other clinical trials or protocols related to breastfeeding.
04

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
46 participants (actual)

Study arms

  • Experimental
    Breastfeeding Computer education

    Breastfeeding Computer education

    Behavioral: Breastfeeding computer education

  • No intervention
    Printed Educational material

    Printed educational material

Interventions

  • BehavioralBreastfeeding computer education

    Breastfeeding computer education

05

What researchers measure

Primary outcomes

  1. Breastfeeding Assessment

    Questionnaire Breastfeeding duration (Specify time) __________

    Time frame: 0-6 months

06

Results

Posted Jun 19, 2019

Participant flow

There were 46 mothers included in the study.

Participant flow — Overall Study
MilestoneComputer Based Breast-feeding Education GroupControl Group
Started2323
Completed2323
Not completed00

Outcome measures

PrimaryBreastfeeding Assessment

Questionnaire Breastfeeding duration (Specify time) __________

Time frame:
0-6 months
Reported as:
Mean · days
Breastfeeding Assessment
daysComputer Based Breast-feeding Education GroupControl Group
Breastfeeding Assessment121.2 ± 65.9120.3 ± 61.8

Adverse events

Collected over 6 months per participant. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Computer Based Breast-feeding Education Group0/23 (0%)0/23 (0%)0/23 (0%)
Control Group0/23 (0%)0/23 (0%)0/23 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Breastfeeding Computer EducationPrinted Educational MaterialTotal
<=18 years000
Between 18 and 65 years232346
>=65 years000
Sex: Female, Male
Sex: Female, Male(Participants)Breastfeeding Computer EducationPrinted Educational MaterialTotal
Female232346
Male000
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Breastfeeding Computer EducationPrinted Educational MaterialTotal
Hispanic or Latino232346
Not Hispanic or Latino000
Unknown or Not Reported000
Region of Enrollment
Region of Enrollment(participants)Breastfeeding Computer EducationPrinted Educational MaterialTotal
United States232346
07

Study locations

1 site
  • University of Nebraska Medical Center, Regional West Medical Center
    Scottsbluff, Nebraska 69361, United States
08

References and documents

Publications

  • Thompson DA, Joshi A, Hernandez RG, Jennings JM, Arora M, Ellen JM. Interactive nutrition education via a touchscreen: is this technology well received by low-income Spanish-speaking parents? Technol Health Care. 2012;20(3):195-203. doi: 10.3233/THC-2012-0669. PubMed 22735734 ↗
  • Thompson DA, Joshi A, Hernandez RG, Bair-Merritt MH, Arora M, Luna R, Ellen JM. Nutrition education via a touchscreen: a randomized controlled trial in Latino immigrant parents of infants and toddlers. Acad Pediatr. 2012 Sep-Oct;12(5):412-9. doi: 10.1016/j.acap.2012.03.020. Epub 2012 Jun 7. PubMed 22682718 ↗
  • Joshi A, Weng W, Lichenstein R, Arora M, Sears A. Prospective tracking of a pediatric emergency department e-kiosk to deliver asthma education. Health Informatics J. 2009 Dec;15(4):282-95. doi: 10.1177/1460458209345899. PubMed 20007653 ↗
  • Joshi A, Arora M, Dai L, Price K, Vizer L, Sears A. Usability of a patient education and motivation tool using heuristic evaluation. J Med Internet Res. 2009 Nov 6;11(4):e47. doi: 10.2196/jmir.1244. PubMed 19897458 ↗
  • Joshi A, Lichenstein R, Rafei K, Bakar A, Arora M. A pilot study to evaluate self initiated computer patient education in children with acute asthma in pediatric emergency department. Technol Health Care. 2007;15(6):433-44. PubMed 18057566 ↗

Study documents

  • Protocol and statistical analysis plan · Mar 5, 2012

Documents are hosted by the registry — open the source record to download them.

09

Registry details

Key details

Study ID
NCT03308058
Lead sponsor
University of Nebraska
Responsible party
Sponsor
First posted
Oct 12, 2017
Start date
Oct 18, 2012
Primary completion
Jan 5, 2018
Completion
Jan 5, 2018
Results posted
Jun 19, 2019
Last update
Sep 28, 2023

Study contacts

Susan Wilhelm, PhD
study chair · University of Nebraska

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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