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ProcrastinationNCT05829174

Comparison of Online Group Therapy Interventions for Procrastination

A study testing Psychoeducation and cognitive modules, Behavioral module: Starting on Time and Planning Realistically and Behavioral module: Working Time Restriction in people with Procrastination, run by Nencki Institute of Experimental Biology of the Polish Academy of Sciences at 1 site in Poland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 26 years
Conditions the study is for
Procrastination
What is being tested?
Psychoeducation and cognitive modules, Behavioral module: Starting on Time and Planning Realistically and Behavioral module: Working Time Restriction
Could I receive a placebo?
No, everyone receives an active treatment
How many people
222 participants
Where
1 sitePoland
Study dates
14 Apr 2023to 15 Jun 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 26 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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
  • Severe personality disorders (with exclusion of avoidant, dependent and obsessive-compulsive personality disorders)

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • Nencki Institute of Experimental Biology, Polish Academy of Sciences

    Warsaw, 02-093

Other trials in Poland

About this study

Official title: Comparison of Online Group Therapy Interventions for Procrastination: A Randomized Controlled Trial With Different Cognitive Behavior Therapy (CBT) Protocols

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.

Conditions
Procrastination
Being tested
Psychoeducation and cognitive modules, Behavioral module: Starting on Time and Planning Realistically, Behavioral module: Working Time Restriction, Behavioral module: Pomodoro Time Management Technique

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Psychoeducation and cognitive modulesBehavioural

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

  • Behavioral module: Starting on Time and Planning RealisticallyBehavioural

    Learning of realistic planning, and timely starting of work.

  • Behavioral module: Working Time RestrictionBehavioural

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

  • Behavioral module: Pomodoro Time Management TechniqueBehavioural

    Working in 25 minutes time intervals

Study groups in NCT05829174
Study groupRoleWhat they receive
Cognitive Behavioral Therapy with Techniques of Starting on Time and Planning RealisticallyExperimental5 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.
Receives: Behavioral: Psychoeducation and cognitive modules; Behavioral: Behavioral module: Starting on Time and Planning Realistically
Cognitive Behavioral Therapy with Technique of Working Time RestrictionExperimental5 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.
Receives: Behavioral: Psychoeducation and cognitive modules; Behavioral: Behavioral module: Working Time Restriction
Cognitive Behavioral Intervention with Time Management TechniqueActive comparator5 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.
Receives: Behavioral: Psychoeducation and cognitive modules; Behavioral: Behavioral module: Pomodoro Time Management Technique
Wait-list control groupNo interventionNo intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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")

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

  2. 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").

    Measured: 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)
  1. Change in Polish version of the Patient Health Questionnaire (PHQ-9)

    Assessment of depressive symptoms. The Polish version of PHQ-9 consists of 9 items that evaluate the occurrence of depressive symptoms in the last 2 weeks (e.g. "Little interest or enjoyment of your activities"). Participants respond on a 4-point Likert scale (0 = "not at all"; 1 = "on a few days"; 2 = "on more than half of the days"; 3 = "nearly every day").

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

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

    Assessment of depressive symptoms. The Polish version of GAD-7 consists of 7 items that evaluate the occurrence of anxiety and excessive worry symptoms in the last 2 weeks (e.g. "Feeling afraid as if something awful might happen"). Participants respond on a 4-point Likert scale (0 = "not at all"; 1 = "on a few days"; 2 = "on more than half of the days"; 3 = "nearly every day").

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

  3. 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).

    Before and after therapy participants will be asked to assess the degree of completion of this project in percents.

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Apr 2023
  2. Study start14 Apr 2023
  3. Primary completion15 Jun 2024
  4. Study completion15 Jun 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
222 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05829174
Sponsor's protocol ID
NenckiInstitute
Status last verified
Nov 2024
First submitted
12 Apr 2023
Last updated
3 Dec 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Psychoeducation and cognitive modules, Behavioral module: Starting on Time and Planning Realistically and Behavioral module: Working Time Restriction in people with Procrastination, run by Nencki Institute of Experimental Biology of the Polish Academy of Sciences at 1 site in Poland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Polish version of the Pure Procrastination Scale (PPS) (time frame: baseline assessment (week 0); mid-treatment assessment (week 3); post-treatment assessment (week 6); follow-up assessment (6 months after post-treatment assessment)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Dec 2024.

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