NCT06814197

Brief Summary

The goals of this clinical trial are to assess the feasibility and efficacy of a one-to-one, layperson-delivered, online Motivational Interviewing (MI) and Cognitive Behavioral Therapy (CBT) intervention for adults aged 18 to 64 experiencing severe procrastination but without moderate-to-severe anxiety or depression. The main questions it aims to answer are:

  • Can a layperson-delivered, online MI and CBT intervention effectively reduce procrastination compared to a waitlist control group?
  • Can the intervention effectively improve self-efficacy and life satisfaction?
  • Are the effects of the intervention maintained one month after completion? Eligible participants will be randomly assigned to either the Intervention group or the Waitlist Control group, with baseline procrastination, self-efficacy, and life satisfaction measured beforehand. Participants in the intervention group will attend four weekly 60-minute online sessions delivered by trained lay coaches supervised by experienced specialists. Sessions will focus on goal-setting, identifying triggers, improving time management, and creating long-term plans to sustain progress. At the end of the intervention, 12 participants will be interviewed to share their experiences. Participants in the waitlist control group will continue their usual activities for four weeks and will receive the same intervention after completing the study assessments. This group will serve as a comparison to evaluate the effectiveness of the intervention.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
117

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

January 17, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

January 23, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

February 7, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 27, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 27, 2025

Completed
Last Updated

July 3, 2025

Status Verified

June 1, 2025

Enrollment Period

4 months

First QC Date

January 17, 2025

Last Update Submit

June 30, 2025

Conditions

Keywords

ProcrastinationMotivational InterviewingCognitive Behavioural TherapyBehaviour ChangeCBTMIRandomised Controlled TrialRCTLay CounsellingTeletherapyeHealthCoaching

Outcome Measures

Primary Outcomes (1)

  • Change in Irrational Procrastination Scale (IPS)

    Irrational Procrastination Scale is a self-report questionnaire measuring procrastination with 9 items on a 5-point Likert scale from 1 (Very Self or Not True of Me) to 5 (Very Often True, or True of Me). The total score is obtained by adding up the scores of each response, with three items reverse-coded. The total score ranges from 9 to 45. IPS has good internal consistency, strong reliability and concurrent validity for use across diverse populations. administered at sign-up, post-intervention, and at one-month follow-up to monitor the effectiveness of the intervention.

    From enrolment to one-month follow-up (8 weeks in total).

Secondary Outcomes (2)

  • Change in General Self-Efficacy Scale (GSE)

    From enrolment to one-month follow-up (8 weeks in total).

  • Change in Cantril Ladder

    From enrolment to one-month follow-up (8 weeks in total).

Other Outcomes (6)

  • Enrollment rate

    From the screening call to the time of enrolment in the study, with follow-up for up to 2 weeks after the screening call.

  • Eligibility rate

    From the screening call to when eligibility is confirmed, within 2 days after the screening call.

  • Attrition

    From enrolment to post-intervention interview (5 weeks in total).

  • +3 more other outcomes

Study Arms (2)

Motivational Interviewing and Cognitive Behavioural Therapy for Procrastination

EXPERIMENTAL

A 4-week intervention will be delivered remotely via Zoom or Google Meets, guided by Overcome coaches. Coaches are trained over two days via training slides, role plays and feedback. The intervention incorporates Motivational Interviewing and Cognitive Behavioural Therapy.

Behavioral: Motivational Interviewing and Cognitive Behavioural Therapy for Procrastination

Waitlist Control

NO INTERVENTION

Participants will be on the waitlist for four weeks and complete outcome measures. After they have completed the outcome measures and concluded their participation in the study, they will receive the intervention too.

Interventions

This intervention incorporates Motivational Interviewing (e.g., open-ended questions, affirmations, reflective listening, summarising) and Cognitive Behavioural Therapy (e.g., cognitive restructuring) techniques in natural conversations instead of having a fully manualised programme. This approach resembles coaching instead of traditional therapy to build therapeutic relationships naturally and keep clients engaged with genuine human connection.

Motivational Interviewing and Cognitive Behavioural Therapy for Procrastination

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Aged 18 to 64.
  • Access to a computer or mobile device with internet connectivity.
  • Ability to understand and speak English.
  • IPS score ≥ 32 to confirm severe procrastination.
  • PHQ-9 score \< 15 to exclude moderate-to-severe depressive symptoms.
  • GAD-7 score \< 12 to exclude moderate-to-severe anxiety symptoms.

You may not qualify if:

  • Cognitive impairments, significant health conditions or disabilities affecting the ability to provide consent and fully participate.
  • Psychiatric diagnoses requiring specialist care (e.g., schizophrenia, eating disorders, substance misuse). Such participants will be signposted to relevant local services if needed.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Overcome

Arnside, LA5 0DP, United Kingdom

Location

Related Publications (9)

  • Vangsness L, Voss NM, Maddox N, Devereaux V, Martin E. Self-Report Measures of Procrastination Exhibit Inconsistent Concurrent Validity, Predictive Validity, and Psychometric Properties. Front Psychol. 2022 Feb 24;13:784471. doi: 10.3389/fpsyg.2022.784471. eCollection 2022.

    PMID: 35282217BACKGROUND
  • Pollak KI, Alexander SC, Tulsky JA, Lyna P, Coffman CJ, Dolor RJ, Gulbrandsen P, Ostbye T. Physician empathy and listening: associations with patient satisfaction and autonomy. J Am Board Fam Med. 2011 Nov-Dec;24(6):665-72. doi: 10.3122/jabfm.2011.06.110025.

    PMID: 22086809BACKGROUND
  • Otermin-Cristeta S, Hautzinger M. Developing an intervention to overcome procrastination. J Prev Interv Community. 2018 Apr-Jun;46(2):171-183. doi: 10.1080/10852352.2016.1198169.

    PMID: 29485388BACKGROUND
  • Mutter A, Kuchler AM, Idrees AR, Kahlke F, Terhorst Y, Baumeister H. StudiCare procrastination - Randomized controlled non-inferiority trial of a persuasive design-optimized internet- and mobile-based intervention with digital coach targeting procrastination in college students. BMC Psychol. 2023 Sep 12;11(1):273. doi: 10.1186/s40359-023-01312-1.

    PMID: 37700387BACKGROUND
  • Johnson SU, Ulvenes PG, Oktedalen T, Hoffart A. Psychometric Properties of the General Anxiety Disorder 7-Item (GAD-7) Scale in a Heterogeneous Psychiatric Sample. Front Psychol. 2019 Aug 6;10:1713. doi: 10.3389/fpsyg.2019.01713. eCollection 2019.

    PMID: 31447721BACKGROUND
  • Jochmann A, Gusy B, Lesener T, Wolter C. Procrastination, depression and anxiety symptoms in university students: a three-wave longitudinal study on the mediating role of perceived stress. BMC Psychol. 2024 May 16;12(1):276. doi: 10.1186/s40359-024-01761-2.

    PMID: 38755730BACKGROUND
  • Harrer M, Cuijpers P, Schuurmans LKJ, Kaiser T, Buntrock C, van Straten A, Ebert D. Evaluation of randomized controlled trials: a primer and tutorial for mental health researchers. Trials. 2023 Aug 30;24(1):562. doi: 10.1186/s13063-023-07596-3.

    PMID: 37649083BACKGROUND
  • Connolly SM, Vanchu-Orosco M, Warner J, Seidi PA, Edwards J, Boath E, Irgens AC. Mental health interventions by lay counsellors: a systematic review and meta-analysis. Bull World Health Organ. 2021 Aug 1;99(8):572-582. doi: 10.2471/BLT.20.269050. Epub 2021 Apr 29.

    PMID: 34354312BACKGROUND
  • Beutel ME, Klein EM, Aufenanger S, Brahler E, Dreier M, Muller KW, Quiring O, Reinecke L, Schmutzer G, Stark B, Wolfling K. Procrastination, Distress and Life Satisfaction across the Age Range - A German Representative Community Study. PLoS One. 2016 Feb 12;11(2):e0148054. doi: 10.1371/journal.pone.0148054. eCollection 2016.

    PMID: 26871572BACKGROUND

MeSH Terms

Interventions

Motivational InterviewingCognitive Behavioral Therapy

Intervention Hierarchy (Ancestors)

Directive CounselingCounselingMental Health ServicesBehavioral Disciplines and ActivitiesHealth ServicesHealth Care Facilities Workforce and ServicesBehavior TherapyPsychotherapy

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Intervention Group: Participants will receive the intervention immediately. Waitlist Control Group: Participants will be on a four-week waitlist. They will receive the intervention after completing their participation in the study.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 17, 2025

First Posted

February 7, 2025

Study Start

January 23, 2025

Primary Completion

May 27, 2025

Study Completion

May 27, 2025

Last Updated

July 3, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

The researchers decided not to make the IPDs shareable to other researchers outside of Outcome. The access to trial IPD will be limited to the researchers within Overcome for future full-scale research. However, the researchers might reconsider at the end of the study if the results from the thematic analysis and/or statistical analysis would be outside of our predictions.

Locations