Cognitive-Behavioral Therapy for Adults With ADHD: A Qualitative Study

Sponsor
Karolinska Institutet (Other)
Overall Status
Recruiting
CT.gov ID
NCT05037903
Collaborator
(none)
20
1
1
18
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Study Details

Study Description

Brief Summary

This is a qualitative study of participants who have taken part in a randomized controlled trial (RCT) of a new treatment protocol based on cognitive-behavioral therapy for adults with attention deficit/hyperactivity disorder predominantly inattentive presentation. The purpose of the qualitative study is to explore participant perceptions of taking part in the RCT to further develop and improve the new treatment protocol.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive-behavioral therapy
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Cognitive-Behavioral Therapy for Adults With Attention-Deficit/Hyperactivity Disorder Inattentive Presentation: A Qualitative Study
Actual Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cognitive-behavioral therapy

Cognitive-behavioral therapy, including behavioral exercises and homework assignments.

Behavioral: Cognitive-behavioral therapy
Cognitive and behavioral interventions aimed at increasing behavioral activation, and reducing procrastination and inattentive symptoms.

Outcome Measures

Primary Outcome Measures

  1. Qualitative interview data [45-60 minutes]

    Participant responses based on questions posed in an interview

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Principal diagnosis of ADHD inattentive presentation

  • 18 years of age or older

  • If on medication, it needs to be well-established since three months, and

  • Prior psycho-educational intervention

Exclusion Criteria:
  • Intellectual impairment

  • Substance use disorder

  • Difficulties in adherence to medical or other treatment

  • Social and/or psychiatric problems to such an extent that they prevent focusing on treatment, or

  • Simultaneous psychological treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stockholm Health Care Services, Region Stockholm Stockholm Sweden

Sponsors and Collaborators

  • Karolinska Institutet

Investigators

  • Principal Investigator: Benjamin Bohman, Karolinska Institutet

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Benjamin Bohman, Study Principal Investigator, Karolinska Institutet
ClinicalTrials.gov Identifier:
NCT05037903
Other Study ID Numbers:
  • KI-2021-01663
First Posted:
Sep 8, 2021
Last Update Posted:
Aug 17, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 17, 2022