Technology-Based Resources to Increase Uptake of Sexual Health Services for Teens

NCT ID: NCT07064070

Last Updated: 2025-07-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-01

Study Completion Date

2026-12-01

Brief Summary

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Alone time with healthcare providers is vital for adolescents, as recommended by several professional organizations, as it enhances health service utilization, empowers adolescents to manage their health, and facilitates discussions on sensitive issues. Despite its importance, only 40% of adolescents have private conversations with clinicians during visits. mHealth technology offers a promising solution for effective interventions to promote alone time with providers for adolescents, parents, and healthcare providers. This pilot study aims to evaluate the preliminary efficacy of a technology-based intervention designed to increase alone time with providers during well-adolescent visits (WAVs) and its impact on trustworthiness, parent-adolescent communication, sexual risk communication, parental monitoring, and parental support. After providing consent, participants accessed a study website to complete a baseline survey, interact with four modules, and complete a post-test survey one month after WAVs. Surveys assessed alone time, trustworthiness, parent-adolescent communication, sexual risk communication, parental monitoring, and parental support.

Detailed Description

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Background: Alone time with healthcare providers is critical for adolescents; several professional organizations recommend it. Alone time with providers promotes better utilization of health services, empowers adolescents to manage their health, and facilitates discussions on sensitive issues. However, only 40% of adolescents have private conversations with clinicians during visits. The advancement mHealth technology provides an excellent opportunity to deliver effective interventions to promote adolescent/provider alone time with adolescents, parents, and providers.

Objective: This pilot study aims to explore 1) the preliminary efficacy of a technology-based intervention designed to increase Alone time with providers during well-adolescent visits (WAVs) and 2) its impact on trustworthiness, parent-adolescent communication, sexual risk communication, parental monitoring, and parental support before and after the intervention.

Methods: A pre and post test design is utilized. After obtaining consent, participants accessed a study website to complete a baseline survey, interact with four modules, and complete a post-test survey one month after WAVs. Participants completed surveys assessing alone time, trustworthiness, parent-adolescent communication, sexual risk communication, parental monitoring, and parental support. Mixed model analysis and effect sizes for pre- and post-intervention outcomes were employed.

Conditions

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mHealth Intervention

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

participants have accessed to the intervention. Single arm study with pre and post design.
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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participant will interact with four module on a secured website.

The online modules included: General Communication, Talking about Relationships and Sexual Health, Parental Monitoring, and Check-up and Check-in (content focused on the importance of alone time). Modules were in English, Chinese, or Spanish

Group Type EXPERIMENTAL

TRUST

Intervention Type BEHAVIORAL

The four online modules included: General Communication, Talking about Relationships and Sexual Health, Parental Monitoring, and Check-up and Check-in (content focused on the importance of alone time). Modules were in English, Chinese, or Spanish

Interventions

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TRUST

The four online modules included: General Communication, Talking about Relationships and Sexual Health, Parental Monitoring, and Check-up and Check-in (content focused on the importance of alone time). Modules were in English, Chinese, or Spanish

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* The child is between 11 and 17 years old
* The child can read and speak English
* The child has access to the internet (via phone or computer)
* The child has a well-child visit scheduled in the next 6 months.
* Mother could be included if they had an adolescent enrolled in this study
* Mother who speaks and reads English, Cantonese, Mandarin, or Spanish
* Mother has access to the internet.

Exclusion Criteria

* Not have a well-child visit scheduled in the next 6 months.
Minimum Eligible Age

11 Years

Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Centers for Disease Control and Prevention

FED

Sponsor Role collaborator

University of California, San Francisco

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jyu-Lin Chen, PhD

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

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Department of Family Health care Nursing

San Francisco, California, United States

Site Status

Countries

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United States

References

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Chen JL, Raymond-Flesch M, Hoffmann TJ, Lin CX, Xu L, Koester KA. Evaluating the Preliminary Efficacy of the TRUST Intervention on Alone-Time and Communication During Well-Adolescent Visits: Quasi-Experimental Study. JMIR Pediatr Parent. 2025 Sep 8;8:e71433. doi: 10.2196/71433.

Reference Type DERIVED
PMID: 40921058 (View on PubMed)

Provided Documents

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Document Type: Informed Consent Form: Parent inform consent

View Document

Related Links

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Other Identifiers

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U48DP006374 DP20-003: SIP20-00

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

U48DP006374

Identifier Type: NIH

Identifier Source: secondary_id

View Link

20-32013

Identifier Type: -

Identifier Source: org_study_id

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