NCT05829174

Brief Summary

The aim of this study is to compare the efficacy of two cognitive behavior therapy (CBT) protocols for procrastination with an active control protocol including cognitive-behavioral elements and with a wait-list control group. The interventions will be delivered online in group settings. All three protocols include identical psychoeducation and cognitive modules related to procrastination, but will differ in the behavioral modules. The behavioral module in one protocol is focused on starting on time and realistic planning. The second protocol implements working time restriction. The active comparator protocol implements the pomodoro time management technique. The wait-list control group will receive one of the CBT protocols after the period of waiting. It is assumed that all active conditions will be superior to the wait-list control, and that CBT protocols will be superior to the protocol including the time management technique. Primary (procrastination) and secondary (depression and anxiety) measures will be collected prior and after the interventions (or waiting period in wait-list group) and after 6-months in the three active condition groups.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
222

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Apr 2023

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

April 12, 2023

Completed
2 days until next milestone

Study Start

First participant enrolled

April 14, 2023

Completed
11 days until next milestone

First Posted

Study publicly available on registry

April 25, 2023

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2024

Completed
Last Updated

December 3, 2024

Status Verified

November 1, 2024

Enrollment Period

1.2 years

First QC Date

April 12, 2023

Last Update Submit

November 28, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change in Polish version of the Pure Procrastination Scale (PPS)

    Assessment of procrastination level. The Polish version of PPS consists of 12 items that evaluate procrastination conceptualized as a dysfunctional delay (e.g. "I am continually saying I'll do it tomorrow"; "I delay making decisions until it's too late"). Participants respond on a 5-point scale (1 = "very seldom or not true of me"; 2 = "seldom true of me"; 3 = "sometimes true of me"; 4 = "often true of me"; 5 = "very often true of true of me")

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

  • Change in Polish version of the Aitken Procrastination Inventory (API)

    Assessment of academic procrastination level. The Polish version of API consists of 19 items that evaluate the tendency of students to procrastinate in their academic tasks (e.g. "If I had an important project to do, I'd get started on it as quickly as possible", "Getting down to work often takes me a long time."). Participants respond on a 5-point scale (1 = "false"; 2 = "mostly false"; 3 = " sometimes false/sometimes true"; 4 = "mostly true"; 5 = "true").

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

Secondary Outcomes (3)

  • Change in Polish version of the Patient Health Questionnaire (PHQ-9)

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

  • Change in Polish version of the Generalized Anxiety Disorder Questionnaire-7 (GAD-7)

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

  • Degree of completion of a particular project that the participant decided to work on during the training (e.g. a thesis, an essay, a report).

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6)

Other Outcomes (15)

  • Change in Polish version of the subscales Low work discipline and Fear of failure of the Study Problems Questionnaire (SPQ)

    baseline assessment (week 0) mid-treatment assessment (week 3);; post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

  • Change in Polish version of the Sensitivity to Punishment and Sensitivity to Reward Questionnaire - Short Form (SPSRQ-SF)

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

  • Change in Polish version of the Multidimensional-Multiattributional Causality Scale (MMCS)

    baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)

  • +12 more other outcomes

Study Arms (4)

Cognitive Behavioral Therapy with Techniques of Starting on Time and Planning Realistically

EXPERIMENTAL

5 session (one session a week) online group therapy including several psychoeducation and cognitive modules (what is procrastination, role of rewards, work environment, belief identification, cognitive restructuring, relapse prevention) and a behavioral module: realistic planning, timely beginning.

Behavioral: Psychoeducation and cognitive modulesBehavioral: Behavioral module: Starting on Time and Planning Realistically

Cognitive Behavioral Therapy with Technique of Working Time Restriction

EXPERIMENTAL

5 session (one session a week) online group therapy including several psychoeducation and cognitive modules (what is procrastination, role of rewards, work environment, belief identification, cognitive restructuring, relapse prevention) and a behavioral module: working time restriction.

Behavioral: Psychoeducation and cognitive modulesBehavioral: Behavioral module: Working Time Restriction

Cognitive Behavioral Intervention with Time Management Technique

ACTIVE COMPARATOR

5 session (one session a week) online group therapy including several psychoeducation and cognitive modules (what is procrastination, role of rewards, work environment, belief identification, cognitive restructuring, relapse prevention) and a behavioral module: pomodoro technique.

Behavioral: Psychoeducation and cognitive modulesBehavioral: Behavioral module: Pomodoro Time Management Technique

Wait-list control group

NO INTERVENTION

No intervention

Interventions

Psychoeducation and cognitive modules: what is procrastination, role of rewards, work environment, belief identification, cognitive restructuring, relapse prevention.

Cognitive Behavioral Intervention with Time Management TechniqueCognitive Behavioral Therapy with Technique of Working Time RestrictionCognitive Behavioral Therapy with Techniques of Starting on Time and Planning Realistically

Learning of realistic planning, and timely starting of work.

Cognitive Behavioral Therapy with Techniques of Starting on Time and Planning Realistically

Restriction of allowed time for work, and gradual increase of allowed time, if previous time windows where effectively used.

Cognitive Behavioral Therapy with Technique of Working Time Restriction

Working in 25 minutes time intervals

Cognitive Behavioral Intervention with Time Management Technique

Eligibility Criteria

Age18 Years - 26 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Bachelor's and Master's university students
  • Self-reported primary difficulties related to chronic and severe procrastination
  • Serious procrastination problem lasting for at least one year as confirmed during clinical interview
  • Having a postponed/procrastinated project to complete in the course of therapy
  • Willing to participate in the study
  • Fluent in Polish language
  • Computer access and stable Internet connection

You may not qualify if:

  • Current participation in other psychotherapy
  • Change of psychiatric medication during last 12 weeks
  • Severe anxiety or affective disorders and any other severe psychiatric disorders that require other type of specialized care and are primary to procrastination problem (e.g. major depressive episode, social phobia, PTSD, etc.)
  • Active suicidality
  • Psychosis, bipolar disorder
  • Alcohol or substance dependence

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nencki Institute of Experimental Biology, Polish Academy of Sciences

Warsaw, 02-093, Poland

Location

Study Officials

  • Marek Wypych, PhD, DSc

    Nencki Institute of Experimental Biology, Polish Academy of Sciences

    PRINCIPAL INVESTIGATOR
  • Jarosław Michałowski, Prof.

    SWPS University of Social Sciences and Humanities

    PRINCIPAL INVESTIGATOR
  • Joachim Kowalski, PhD

    Institute of Psychology, Polish Academy of Sciences

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 12, 2023

First Posted

April 25, 2023

Study Start

April 14, 2023

Primary Completion

June 15, 2024

Study Completion

June 15, 2024

Last Updated

December 3, 2024

Record last verified: 2024-11

Locations