Can You Reduce Problematic Smartphone Use Through a Group Intervention: A Single Case Experimental Design

NCT ID: NCT05384548

Last Updated: 2022-11-02

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

TERMINATED

Clinical Phase

NA

Total Enrollment

7 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-20

Study Completion Date

2022-10-29

Brief Summary

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This study will develop and conduct an initial, single-case, mixed-methods evaluation of a brief group intervention for mild and moderate problematic phone use.

Detailed Description

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Conditions

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Addiction, Smartphone

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Outcome measures will be collected electronically without involvement of the researchers.

Study Groups

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Problematic smart phone use course

Group Type EXPERIMENTAL

Problematic smart phone use course

Intervention Type BEHAVIORAL

A 6 session, online, group-based, psychological course targetting problematic smart phone use.

Interventions

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Problematic smart phone use course

A 6 session, online, group-based, psychological course targetting problematic smart phone use.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

-Self-identifies as struggling with problematic smart phone use

Exclusion Criteria

* Actively experiencing suicidal or self-injurious thoughts, or have experienced these within the past year
* Already in a psychological therapy/intervention
* Planning a change of psychotropic medication during the research project.
* No access to video calling and/or slow internet connection speed
* A mental health condition that is not currently well managed/stable and therefore other interventions are likely to be more appropriate
* Does not own a smartphone that can record screen time
* Is not living in the UK, with access to services within the UK
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Canterbury Christ Church University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Brett Hayes

Role: PRINCIPAL_INVESTIGATOR

Canterbury Christ Church University

Fergal Jones

Role: STUDY_DIRECTOR

Canterbury Christ Church University

Locations

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Salomons Institute, Canterbury Christ Church University

Royal Tunbridge Wells, Kent, United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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2020_Brett_Hayes_MRP

Identifier Type: -

Identifier Source: org_study_id

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