NCT05384548

Brief Summary

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.

Trial Health

57
Monitor

Trial Health Score

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

Enrollment
7

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 17, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 20, 2022

Completed
Same day until next milestone

Study Start

First participant enrolled

May 20, 2022

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 29, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 29, 2022

Completed
Last Updated

November 2, 2022

Status Verified

October 1, 2022

Enrollment Period

5 months

First QC Date

May 17, 2022

Last Update Submit

October 31, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change from pre-intervention (week 1) at post-intervention (week 10) on the Smartphone Addiction Scale -Short Version (SAS-SV).

    This measures smartphone addiction producing a score between 10 and 60, with higher scores indicating greater levels of addiction.

    Post-intervention (week 10)

Secondary Outcomes (9)

  • Change from pre-intervention (week 1) at follow-up (week 18) on the Smartphone Addiction Scale -Short Version (SAS-SV).

    Follow-up (week 18)

  • Change from pre-intervention (week 1) at post-intervention (week 10) on the Depression, Anxiety and Stress Scale -21 item version (DASS-21).

    Post-intervention (week 10)

  • Change from pre-intervention (week 1) at follow-up (week 18) on the Depression, Anxiety and Stress Scale -21 item version (DASS-21).

    Follow-up (week 18)

  • Change from pre-intervention (week 1) at post-intervention (week 10) on the Multicultural Quality of Life Index.

    Post-intervention (week 10)

  • Change from pre-intervention (week 1) at follow-up (week 18) on the Multicultural Quality of Life Index.

    Follow-up (week 18)

  • +4 more secondary outcomes

Other Outcomes (1)

  • Qualitative interview

    Week 18

Study Arms (1)

Problematic smart phone use course

EXPERIMENTAL
Behavioral: Problematic smart phone use course

Interventions

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

Problematic smart phone use course

Eligibility Criteria

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

You may qualify if:

  • Self-identifies as struggling with problematic smart phone use

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Salomons Institute, Canterbury Christ Church University

Royal Tunbridge Wells, Kent, TN1 2YG, United Kingdom

Location

MeSH Terms

Conditions

Internet Addiction Disorder

Condition Hierarchy (Ancestors)

Technology AddictionBehavior, AddictiveCompulsive BehaviorImpulsive BehaviorBehavior

Study Officials

  • Brett Hayes

    Canterbury Christ Church University

    PRINCIPAL INVESTIGATOR
  • Fergal Jones

    Canterbury Christ Church University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Outcome measures will be collected electronically without involvement of the researchers.
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 17, 2022

First Posted

May 20, 2022

Study Start

May 20, 2022

Primary Completion

October 29, 2022

Study Completion

October 29, 2022

Last Updated

November 2, 2022

Record last verified: 2022-10

Data Sharing

IPD Sharing
Will not share

Locations