NCT06278142

Brief Summary

The main purpose of this study is to present the development process and project flow of an internet-based self-help intervention programme to reduce the level of procrastination among university students.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable

Status
not yet recruiting

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

February 19, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 26, 2024

Completed
4 days until next milestone

Study Start

First participant enrolled

March 1, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2024

Completed
Last Updated

February 26, 2024

Status Verified

February 1, 2024

Enrollment Period

1 month

First QC Date

February 19, 2024

Last Update Submit

February 19, 2024

Conditions

Keywords

Web-based interventionCognitive Behavioral TherapyProcrastination

Outcome Measures

Primary Outcomes (4)

  • Tuckman Procrastination Behaviour Scale

    Turkish adaptation of the scale consists of 14 items, five-point Likert type (1: strongly disagree-5: strongly agree) and one dimension. The evaluation of the Tuckman Procrastination Behaviour scale is made by taking the average of all items. The maximum score that can be obtained from the scale is expressed as five and the minimum score as one.

    Time Frame: Pre-test, post-test (5 weeks later from pre-test), follow up (10 weeks later from pre-test)

  • Cognitive Distortions Questionnaire

    Turkish adaptation of the form was developed by Batmaz et al. (2015) and consists of 15 items of 9 Likert type. The scale items can be used in short and ultra short form.The 9-item short form will be used to collect data from the study group. The 9-item short form will be used to collect data from the study group.

    Time Frame: Pre-test, post-test (5 weeks later from pre-test), follow up (10 weeks later from pre-test)

  • Time Management Scale

    The lowest score that can be obtained from the scale is 27 and the highest score is 135 (Alay \& Koçak, 2002). It was deemed appropriate for the evaluation of time management skills in the study group.

    Time Frame: Pre-test, post-test (5 weeks later from pre-test), follow up (10 weeks later from pre-test)

  • Attitude Scale for Internet-Based Interventions

    Apolinário-Hagen et al. (2018) is a measurement tool consisting of 16 items adapted into Turkish by Özer et al. (in the publication stage). Scale consists of two sub-dimensions named as "Perceived Usefulness and Usefulness" and "Relative Advantage and Comparability".

    Time Frame: Pre-test, post-test (5 weeks later from pre-test), follow up (10 weeks later from pre-test)

Secondary Outcomes (1)

  • Depression Anxiety Stress Scale-21 (DASS-21)

    Time Frame: Pre-test, post-test (5 weeks later from pre-test), follow up (10 weeks later from pre-test)

Other Outcomes (1)

  • Sociodemographic Information Form

    [Time Frame: Pre-test]

Study Arms (3)

Guided Web-Based Intervention

EXPERIMENTAL

Participants in this group will use the web-based intervention with guidance support.

Other: Internet Based Intervention - GUIDED

Without Guidance Web-Based Intervention

EXPERIMENTAL

Participants in this group will use the web-based intervention without guidance support.

Other: Internet Based Intervention - WİTHOUT GUİDANCE

Waitlist

NO INTERVENTION

Participants will have no contact with the study team during the waiting period.

Interventions

In the expert-supported application, each participant will be sent a folder to be shared by the user and the guide via Google Drive, and the user is expected to perform the application in the folder. A module is added to the folder every Monday and the participant is asked to complete the relevant module until Friday of the same week. In the following two days, a feedback message is provided by the expert, taking into account the user's responses.

Guided Web-Based Intervention

The developed implementation plan is communicated to the participants without expert support and their participation is ensured. A common folder will be created with the participants accepted to the study and in the group without expert support, and the process is managed by transmitting the module to the user via the folder every Monday.

Without Guidance Web-Based Intervention

Eligibility Criteria

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

You may qualify if:

  • volunteering to participate in the study
  • being 18 years of age or older
  • being an undergraduate student
  • having internet access and an e-mail address with gmail extension
  • getting a score above 3.5 points from the Tuckman Procrastination Behaviour Scale, having a score lower than 20 points for the depression sub-dimension, 15 points for the anxiety sub-dimension and 19 points for the stress sub-dimension of the DASS 21 scale (the participant is expected to meet all sub-dimension conditions).

You may not qualify if:

  • not being in a psychological help process
  • not having any psychiatric diagnosis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Counseling

Intervention Hierarchy (Ancestors)

Mental Health ServicesBehavioral Disciplines and ActivitiesCommunity Health ServicesHealth ServicesHealth Care Facilities Workforce and Services

Central Study Contacts

Ömer Özer, Phd

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 19, 2024

First Posted

February 26, 2024

Study Start

March 1, 2024

Primary Completion

April 1, 2024

Study Completion

July 1, 2024

Last Updated

February 26, 2024

Record last verified: 2024-02