A Family Literacy Program for Latino Families
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|ClinicalTrials.gov Identifier: NCT03941197|
Recruitment Status : Enrolling by invitation
First Posted : May 7, 2019
Last Update Posted : June 17, 2019
|Condition or disease||Intervention/treatment||Phase|
|Literacy||Behavioral: Ready and Healthy for Kindergarten Family Literacy program||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||30 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Ready and Healthy for Kindergarten- A Family Literacy Program for Latino Families|
|Actual Study Start Date :||May 28, 2019|
|Estimated Primary Completion Date :||September 2019|
|Estimated Study Completion Date :||December 2019|
Experimental: Ready and Healthy for Kindergarten Family Literacy Program
Ready and Healthy for Kindergarten Family Literacy Program- 8 weekly parent child workshops with text message reminders
Behavioral: Ready and Healthy for Kindergarten Family Literacy program
Participants will participate in 8 parent-child health-themed literacy workshops. Participants will receive 2-3 text messages per week for 8 weeks.
- Acceptability of Intervention Measure (AIM) Questionnaire [ Time Frame: After 8 week period. ]Acceptability will be measured using the Acceptability of Intervention Measure (AIM). The AIM consists of 4 questions that assess acceptability. Responses range from 1 (completely disagree) to 5 (completely agree). Scales are created by averaging responses.
- StimQ-Preschool survey [ Time Frame: At enrollment and after 8 week period. ]Parent reported measure of the cognitive home environment for children 5 months to 6 years to assess aspects of the home environment that affect child development.
- Alphabet knowledge assessment survey [ Time Frame: At enrollment and after 8 week period. ]Alphabet knowledge will be assessed.
- Sight word knowledge assessment survey [ Time Frame: At enrollment and after 8 week period. ]Sight word knowledge will be assessed
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03941197
|United States, New Jersey|
|Manuel E Jimenez|
|New Brunswick, New Jersey, United States, 08901|
|Principal Investigator:||Manuel E Jimenez, MD, MS||Rutgers Robert Wood Johnson Medical School|