ClinicalTrials.gg
CompletedNCT03659279Updated Oct 26, 2018

Let's Get Organized Feasibility Study

An interventional study of Let's Get Organized in Neurodevelopmental Disorders and Mental Disorder, sponsored by Örebro University, Sweden. Completed. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2018-10-26.

Sponsored by Örebro University, Sweden · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 5 months after the study started (first participant enrolled Mar 2015, registered Aug 2018).
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of this study is to pilot test the Let's Get Organized (LGO) Occupational Therapy intervention in a Swedish context by exploring possible enhancements in time management skills, aspects of executive functioning, and satisfaction with daily occupations in persons with time-management difficulties due to neurodevelopmental and/or mental disorders.

Method:

A pre-post design with 3 and 12-months follow-up is used.

The LGO intervention is a manual-based group intervention aiming to enhance time-management, targeted to persons with mental or neurodevelopmental disorders. The LGO is conducted as 10 weekly 1.5-hour group sessions. Two trained group leaders, lead each group of 6-8 participants. Goal-directed and other learning strategies are used to train effective time management habits such as maintaining a calendar and wearing a watch. All group sessions follow the same format, and each session has a set theme. Group sessions are structured with a slide presentation and a course manual, and information from the group leaders is intermixed with discussion among the participants and tasks to complete.

The primary outcome of the study is self-reported time management measured by the Assessment of Time Management Skills (ATMS-S). Secondary outcomes are executive functioning measured with the Weekly Calendar Planning Activity (WCPA) and satisfaction with daily occupations, which is measured with the interview-administered questionnaire Satisfaction with Daily Occupations 13 items (SDO-13).

Data will be collected before intervention start (pre intervention), after intervention completion (post intervention) and 3 and 12 months post intervention completion. The ATMS will be collected at all four time points. The WCPA and SDO-13 will be collected pre, post and 12 months post intervention.

02

Conditions studied

  • Neurodevelopmental Disorders
  • Mental Disorder

Keywords

  • Time management
  • Group intervention
  • Executive function
03

In context

Neurodevelopmental Disorders

336 studies on the registry are indexed under Neurodevelopmental Disorders; 141 are open to participants now.

This study's enrollment of 75 is below the median of 89 across 208 interventional studies indexed under Neurodevelopmental Disorders.

Browse Neurodevelopmental Disorders studies →

Lead sponsor

Örebro University, Sweden is the lead sponsor of 86 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • confirmed or suspected diagnosis of a mental disorder, such as affective disorder or schizophrenia, or neurodevelopmental disorder, such as autism spectrum disorder or attention deficit hyperactivity disorder/attention deficit disorder
  • self-reported difficulties in time management in daily life to an extent that affects functioning in daily life negatively

Exclusion criteria

Exclusion Criteria:

  • intellectual disability
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
75 participants (actual)

Study arms

  • Experimental
    Let's Get Organized

    Group intervention with 10 weekly sessions, each lasting 1.5 hours.

    Behavioral: Let's Get Organized

Interventions

  • BehavioralLet's Get Organized

    Group intervention aiming to enhance time-management, targeted to persons with mental or neurodevelopment disorders. Each group has 6-8 participants and is lead by two trained group leaders. Goal-directed and other learning strategies are used to train effective time management habits such as maintaining a calendar and wearing a watch. Group sessions are structured with a PowerPoint presentation and a course manual, and information from the group leaders is intermixed with discussion among the participants and tasks to complete.

    Also known as: LGO

06

What researchers measure

Primary outcomes

  1. Change Assessment of Time Management Skills (ATMS-S) Time management sub scale

    Time management (11 items) measured in ATMS units (range 0-100)

    Time frame: baseline (pre-intervention), 10 weeks, 24 weeks, 62-months

Secondary outcomes

  1. Change in Weekly Calendar Planning Activity (WCPA-SE) No of appointments

    No of correctly entered appointments (range 0-17) Total time No of strategies used No of rules followed (0-5)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  2. Change in Weekly Calendar Planning Activity (WCPA-SE) Total time

    Total time No of strategies used No of rules followed (0-5)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  3. Change in Weekly Calendar Planning Activity (WCPA-SE) Strategies

    No of strategies used No of rules followed (0-5)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  4. Change in Weekly Calendar Planning Activity (WCPA-SE) Rules followed

    No of rules followed (range 0-5)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  5. Change in Satisfaction with Daily Occupations 13 items (SDO-13) Activity sub scale

    No of activities (range 0-13)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  6. Change in Satisfaction with Daily Occupations 13 items (SDO-13) Satisfaction sub scale

    Satisfaction sub scale score (each item is scored 1-7 and summed to a sub scale score, range 13-91, higher score indicates better satisfaction)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  7. Change in Satisfaction with Daily Occupations 13 items (SDO-13) Global satisfaction sub scale

    Global satisfaction score (range 1-5, lower score indicates better satisfaction)

    Time frame: baseline (pre-intervention), 10 weeks, 62-months

  8. Change in Assessment of Time Management Skills (ATMS-S) Organization and planning sub scale

    Organization and Planning (11 items) measured in ATMS units (range 0-100)

    Time frame: baseline (pre-intervention), 10 weeks, 24 weeks, 62-months

  9. Change in Assessment of Time Management Skills (ATMS-S) Regulation of emotions sub scale

    Regulation of emotions (5 items) measured in ATMS units (range 0-100)

    Time frame: baseline (pre-intervention), 10 weeks, 24 weeks, 62-months

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Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 26, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03659279
Lead sponsor
Örebro University, Sweden
Collaborators
Dalarna County Council, Sweden, Region Örebro County, Uppsala University, Region Gävleborg, State University of New York - Downstate Medical Center
Responsible party
Sponsor
First posted
Sep 6, 2018
Start date
Mar 1, 2015
Primary completion
Jun 2016
Completion
Jun 2017
Last update
Oct 26, 2018

Study contacts

Marie Holmefur, PhD
principal investigator · Örebro University, Sweden

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2018. You cannot join it, but the record below documents what was studied.

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