NCT06157710

Brief Summary

The aim of this study is to evaluate the effect of an 8-week self-directed internet based CBT intervention on various psychological outcomes for young students struggling with procrastination in the UK. The psychological outcomes consist of motivation, depressive symptoms, impulsivity and anxiety. More specifically, the study aims to compare the effect of the intervention vs waitlist control at 8 weeks on primary and secondary outcomes. Additionally, the study aims to explore whether changes in primary and secondary outcomes as the result of the intervention are mediated or moderated by key intervention processes.

Trial Health

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Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

First Submitted

Initial submission to the registry

November 27, 2023

Completed
4 days until next milestone

Study Start

First participant enrolled

December 1, 2023

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 6, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2024

Completed
Last Updated

May 9, 2024

Status Verified

May 1, 2024

Enrollment Period

7 months

First QC Date

November 27, 2023

Last Update Submit

May 7, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Procrastination: Pure Procrastination Scale (PPS; Rozental, Forsell, et al., 2014)

    measures procrastination by using 12 items to detect and determine dysfunctional delay. The higher the score the more likely the individual is to delay an activity or task

    Baseline, WK4, WK8

Secondary Outcomes (9)

  • Demographics

    Baseline

  • Clinical Perfectionism Questionnaire (CPQ) (Fairburn et al., 2003)

    Baseline, WK4, WK8

  • Depressive symptoms: Patient health questionnaire-8 (PHQ-8) (Kroenke et al., 2008)

    Baseline, WK4, WK8

  • Anxiety symptoms: General Anxiety Disorder Scale (GAD-7) (Spitzer et al., 2006)

    Baseline, WK4, WK8

  • Impulsivity: Short form Barratt Impulsiveness Scale (Spinella 2009)

    Baseline, WK4, WK8

  • +4 more secondary outcomes

Study Arms (2)

Procrastinate digital programme

EXPERIMENTAL

8-week unternet-based CBT for procrastination * Behavioural Module: Introduction * Behavioural Module: Goal setting techniques * Behavioural Module: Motivation * Behavioural Module: Barriers to action * Behavioural Module: Managing maladaptive thoughts and beliefs * Behavioural Module: Value clarification * Behavioural Module: Moving forward

Behavioral: Digital intervention through modules

Waitlist control

NO INTERVENTION

Wait-list control group. They do not receive the weekly modules though they are asked to complete 4-week and 8-week online surveys. They will be allowed to revive the intervention after 8 weeks.

Interventions

* Introduction * Goal Setting Techniques * Motivation * Barriers to Action * Managing Maladaptive Thoughts and Beliefs * Value Clarification * Moving Forward

Procrastinate digital programme

Eligibility Criteria

Age16 Years - 24 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Resident in the UK
  • Fluent in English
  • Aged between 16 and 24 years of age
  • Have access to computer or smartphone
  • Score at least 40 points on the Pure Procrastination Scale (indicating difficulties with procrastination)

You may not qualify if:

  • Ongoing psychological treatment
  • New course of change in dose of psychotropic medication in the last two months (self-reported)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Bath

Bath, United Kingdom

RECRUITING

Central Study Contacts

Jeffrey Lambert, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr Jeffrey Lambert

Study Record Dates

First Submitted

November 27, 2023

First Posted

December 6, 2023

Study Start

December 1, 2023

Primary Completion

July 1, 2024

Study Completion

September 1, 2024

Last Updated

May 9, 2024

Record last verified: 2024-05

Data Sharing

IPD Sharing
Will not share

Locations