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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05037903
Other study ID # KI-2021-01663
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2021
Est. completion date August 31, 2022

Study information

Verified date February 2023
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date August 31, 2022
Est. primary completion date August 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms

  • Attention Deficit Disorder with Hyperactivity
  • Attention Deficit Hyperactivity Disorder
  • Hyperkinesis

Intervention

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

Locations

Country Name City State
Sweden Stockholm Health Care Services, Region Stockholm Stockholm

Sponsors (1)

Lead Sponsor Collaborator
Karolinska Institutet

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Qualitative interview data Participant responses based on questions posed in an interview 45-60 minutes
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