NCT06750978

Brief Summary

This project proposes to evaluate the feasibility and effects of behavioral intervention strategies on problematic smartphone use among college students. The project proposes to evaluate three behavioral intervention components- self-reflection via actively monitoring phone usage, increasing engagement in non-smartphone activities, and contingency management (i.e., financial incentives) - on short-term and long-term reductions in problematic smartphone use (PSU) among college students. The research team will develop a mobile application, referred to as the app, to collect data on a subject's daily phone usage and activity engagement. The app will comprise three features, with specific sets of features being activated during different phases.

  • Feature 1: The app will autonomously track the time spent on the apps categorized as social media and gaming.
  • Feature 2: The app will display the daily amount of usage on social media and gaming apps, with an option for a subject to confirm their acknowledgment of the daily time spent.
  • Feature 3: The app will display an option for subject to confirm their engagement in the alternative activities as planned.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress93%
Dec 2024Jun 2026

Study Start

First participant enrolled

December 18, 2024

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

December 20, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

December 27, 2024

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

May 22, 2026

Status Verified

May 1, 2026

Enrollment Period

1.5 years

First QC Date

December 20, 2024

Last Update Submit

May 19, 2026

Conditions

Keywords

Problematic smartphone use, smartphone overuse

Outcome Measures

Primary Outcomes (2)

  • Daily smartphone usage data

    The amount of time spent on apps identified by the participants

    8 weeks

  • Problematic smartphone use

    Severity of problematic smartphone use will be assessed with the Smartphone Addiction Scale (SAS) short version. The SAS short version includes 10 items. The sum of these items gives an overall score ranging 10-60, with higher score indicating more severe problematic smartphone use.

    8 weeks

Study Arms (3)

Self-reflection

EXPERIMENTAL

Participants actively review their smartphone usage data each day, which will be verified by the app.

Behavioral: Self-reflection

Self-reflection + Contingency management

EXPERIMENTAL

Participants will actively review their smartphone usage each day, which will be verified via the app. If the participant meets their daily PSU reduction goal, they will receive an incentive ($8); if they do not meet their goal, they will receive nothing.

Behavioral: Self-reflection + Contingency management

Control

NO INTERVENTION

Participants will not engage in any behavioral intervention strategies

Interventions

Self-reflectionBEHAVIORAL

Participants will be guided to identify goals of daily PSU reduction. o Participants will be guided to actively review their smartphone usage data each day.

Self-reflection

Participants will be guided to identify goals of daily PSU reduction and actively review their smartphone usage data each day. Participants will receive an incentive ($8) if they meet the daily PSU reduction goal.

Self-reflection + Contingency management

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Rutgers students who are 18+ years old
  • Use an Android smartphone
  • identified as having problematic smartphone use (scored 31+ on the Smartphone Addiction Scale)

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rutgers University

New Brunswick, New Jersey, 08817, United States

Location

Study Officials

  • Wen Anthony, PhD

    Rutgers University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: A randomized controlled trial with repeated measures design will be used. The study consists of three phases. (1) Baseline phase (2 weeks): Following eligibility screening and consent, all participants will install an app developed by the research team. The app will track and report participants daily smartphone usage and establish a baseline pattern of PSU. (2) Experimental phase (4 weeks): After the baseline data collection, participants will be randomized on a rolling basis into one of the three conditions: Self-Reflection (n=20), Self-Reflection (n=20) + Contingency Management (n=10), and Control. Participants daily smartphone usage, review of usage data, and/or evidence of alternative activity engagement will be recorded by the app and reported to the researcher. (3) Follow-up phase (2 weeks): The two intervention conditions will be withdrawn in this phase.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

December 20, 2024

First Posted

December 27, 2024

Study Start

December 18, 2024

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

May 22, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

IPD will not be shared due to concerns about maintaining participant privacy and confidentiality. Although measures such as data anonymization can reduce re-identification risks, complete elimination of such risks cannot be guaranteed. Additionally, the consent forms used in this study do not include provisions for IPD sharing. To comply with ethical guidelines and regulatory standards, we have decided not to share IPD at this time.

Locations