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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03281356
Other study ID # Pro20170000402
Secondary ID
Status Completed
Phase N/A
First received September 11, 2017
Last updated September 11, 2017
Start date May 9, 2017
Est. completion date June 13, 2017

Study information

Verified date September 2017
Source Rutgers, The State University of New Jersey
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date June 13, 2017
Est. primary completion date June 13, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
United States Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Rutgers, The State University of New Jersey

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability Survey Three questions on the participants feedback on the program. Visit 2 (1 month)
Secondary Stim Q Survey The StimQ is a parent reported measure of the cognitive home environment Visit 2 (1 month)
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