Efficacy of an Occupational Intervention for Improving Quality of Work Life in Adults Living With ADHD

Last updated: May 13, 2025
Sponsor: Université du Québec a Montréal
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Williams Syndrome

Attention Deficit/hyperactivity Disorder (Adhd - Adults)

Treatment

Minds@Work-ADHD-Quality of Life

Minimal contact

Clinical Study ID

NCT06774378
2023-0SYA-312580
  • Ages > 18
  • All Genders

Study Summary

An adaptation of the Minds@Work intervention to improve quality of life at work for adults living with attention deficit disorder with/without hyperactivity (ADHD), following a group format.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age ≥ 18 years

  • French language proficiency

  • Score ≤ 4 on Part A of the Adult ADHD Self-Report Scale (ASRS-v1.1)

  • Currently employed

  • Express desire to improve Quality of Work Life (QoWL)

Exclusion

Exclusion Criteria:

  • Currently receiving psychosocial services (e.g., psychotherapy, occupationaltherapy) specifically targeting QoWL improvement

Study Design

Total Participants: 60
Treatment Group(s): 2
Primary Treatment: Minds@Work-ADHD-Quality of Life
Phase:
Study Start date:
August 28, 2024
Estimated Completion Date:
May 31, 2025

Study Description

In this study, the research team has developed a psychosocial group intervention specifically aimed at improving quality of life at work for ADHD workers. Work-related themes cover motivation, accommodations, problem solving, cognitive functions (i.e. attention and memory), hyperactivity and impulsivity, interpersonal interactions, and medication management.

The general objective of this project is to evaluate the effectiveness of this new psychosocial intervention aimed at improving the quality of life at work of workers living with ADHD, using a randomized controlled trial design.

More specifically, the project will aim to:

Objective #1: Evaluate the effectiveness of the intervention on the quality of life at work of workers living with ADHD (primary outcome).

Objective #2: Evaluate the effectiveness of the intervention on secondary variables, namely the satisfaction of psychological needs, job satisfaction, well-being at work, self-esteem as a worker, occupational self-efficacy, cognitive functioning, self-compassion and the quality of the relationship with members of the workplace (secondary outcomes).

  • Hypothesis #1: There will be a statistically significant improvement in the quality of life at work between the pre- and post-intervention measurements in participants receiving the experimental condition.

  • Hypothesis #2: There will be a statistically significant condition*time interaction indicating that the improvement in quality of work life among participants receiving the experimental condition between the pre- and post-intervention measurement times will be greater than that of the control condition.

  • Hypotheses #3 to 10: There will be a statistically significant improvement in the secondary outcomes mentioned above between the pre- and post-intervention measurements among participants receiving the experimental condition.

  • Hypothesis #11: For participants receiving the experimental condition, there will be no statistically significant difference in quality of work life between the follow-up times, indicating that the gains acquired during the intervention will be maintained at 3, 6, 9, and 12 months.

Our research team collaborates with the PANDA Les Deux-Rives association, which is a non-profit organization specializing in ADHD. The psychosocial intervention was co-designed, which allows the involvement of field stakeholders in all stages of the research. This involvement promotes the creation of a final research output that will meet the needs of the target population and that will be easily implemented in the organizational structures already in place.

Connect with a study center

  • Université du Québec à Montréal

    Montréal, Quebec H2X 3R9
    Canada

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.