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Text Messaging Pilot Study

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ClinicalTrials.gov Identifier: NCT03281356
Recruitment Status : Completed
First Posted : September 13, 2017
Last Update Posted : September 13, 2017
Sponsor:
Information provided by (Responsible Party):
Manuel E. Jimenez, MD, MS, Rutgers, The State University of New Jersey

Brief Summary:
This pilot study aims to assess the acceptability, feasibility, and preliminary effectiveness of text messages designed to encourage shared reading among urban parents. We hypothesize that parents will report reading more often to their children after receiving the text messages.

Condition or disease Intervention/treatment Phase
Literacy Behavioral: Intervention Group Not Applicable

Detailed Description:
This is a single arm, pilot study. The participants enrolled will receive two text messages per week for a 4 week period (a total of 8 messages). At the end of the study period we will assess change in number of reading occurrences using a validated measure. Parents will also complete a brief acceptability survey.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 16 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Text Messaging Pilot Study to Encourage Shared Reading Among a Sample of Urban Parents.
Actual Study Start Date : May 9, 2017
Actual Primary Completion Date : June 13, 2017
Actual Study Completion Date : June 13, 2017

Arm Intervention/treatment
Experimental: Intervention Group Behavioral: Intervention Group
Participants will receive a total of 8 text messages during a 4 week period.




Primary Outcome Measures :
  1. Acceptability Survey [ Time Frame: Visit 2 (1 month) ]
    Three questions on the participants feedback on the program.


Secondary Outcome Measures :
  1. Stim Q Survey [ Time Frame: Visit 2 (1 month) ]
    The StimQ is a parent reported measure of the cognitive home environment



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Preferred language either English or Spanish,
  2. Parent or legal guardian,
  3. Age ≥ 18,
  4. Willing to accept text messages

Exclusion Criteria:

  1. Individuals unable to provide consent
  2. Individuals who do not meet inclusion criteria

Information from the National Library of Medicine

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): NCT03281356


Locations
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United States, New Jersey
Rutgers Robert Wood Johnson Medical School
New Brunswick, New Jersey, United States, 08901
Sponsors and Collaborators
Rutgers, The State University of New Jersey
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Responsible Party: Manuel E. Jimenez, MD, MS, Assistant Professor, Rutgers, The State University of New Jersey
ClinicalTrials.gov Identifier: NCT03281356    
Other Study ID Numbers: Pro20170000402
First Posted: September 13, 2017    Key Record Dates
Last Update Posted: September 13, 2017
Last Verified: September 2017

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Manuel E. Jimenez, MD, MS, Rutgers, The State University of New Jersey:
Pilot Study
Early childhood development