The Effects of Peer Co-led Educational Group Intervention for Adults With Attention-Deficit Hyperactivity Disorder

NCT ID: NCT03547843

Last Updated: 2022-01-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

56 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-05-31

Study Completion Date

2020-03-15

Brief Summary

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Peer co-led education describes educators who are expert patients, user representatives or former patients, participating and teaching in educational interventions in cooperation with health care professionals. Peer co-led education is included in the Norwegian national guidelines for treatment of mental disorders, but despite some promising results for the treatment of other conditions, still little is known about the efficacy of peer co-led educational group interventions interventions for adults with attention deficit and hyperactivity disorder (ADHD).

This pilot trial will evaluate patient satisfaction with and preliminary efficacy of a 2-session peer co-led educational group program designed to address specific challenges faced by adults diagnosed with ADHD at an outpatient clinics in mid-Norway.

Detailed Description

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Conditions

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Attention Deficit Disorder With Hyperactivity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Pilot randomized clinical trial
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Educational intervention

Patients randomized to the intervention group will start with a group-based educational program immediately after the randomization.

Group Type EXPERIMENTAL

Group-based education

Intervention Type BEHAVIORAL

The group-based educational program consists of two sessions that run over two consecutive weeks. Each session consists of a lecture from a recruited expert on the topic of the session and by expert patients with a following discussion of the topic facilitated by the course leader.

Standard treatment

Intervention Type OTHER

Diagnostic treatment with medication. In addition, some patients receive cognitive behavioral therapy (not systematically given to every patient). If needed, patients are also offered assistance with regard to economy, housing, education, and work as well as contact with family and network.

Waiting list

Participants randomized to the waiting list control group receive no educational intervention for the duration of the 10 weeks. During this period participants can receive standard treatment, consisting of diagnostic treatment with medication.

Group Type ACTIVE_COMPARATOR

Waiting list

Intervention Type BEHAVIORAL

No educational intervention for the duration of the 10 weeks. During this period participants can receive standard treatment.

Standard treatment

Intervention Type OTHER

Diagnostic treatment with medication. In addition, some patients receive cognitive behavioral therapy (not systematically given to every patient). If needed, patients are also offered assistance with regard to economy, housing, education, and work as well as contact with family and network.

Interventions

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Group-based education

The group-based educational program consists of two sessions that run over two consecutive weeks. Each session consists of a lecture from a recruited expert on the topic of the session and by expert patients with a following discussion of the topic facilitated by the course leader.

Intervention Type BEHAVIORAL

Waiting list

No educational intervention for the duration of the 10 weeks. During this period participants can receive standard treatment.

Intervention Type BEHAVIORAL

Standard treatment

Diagnostic treatment with medication. In addition, some patients receive cognitive behavioral therapy (not systematically given to every patient). If needed, patients are also offered assistance with regard to economy, housing, education, and work as well as contact with family and network.

Intervention Type OTHER

Other Intervention Names

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Patient education Treatment as usual

Eligibility Criteria

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Inclusion Criteria

* Confirmed ADHD-diagnosis
* speaking a Scandinavian language

Exclusion Criteria

* Unable to give informed consent
* Psychosis
* Severe learning difficulties
Minimum Eligible Age

18 Years

Maximum Eligible Age

67 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Olavs Hospital

OTHER

Sponsor Role collaborator

Norwegian University of Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Anne-Lise Løvaas, md phd

Role: STUDY_DIRECTOR

St. Olavs Hospital

Locations

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Tiller DPS

Trondheim, , Norway

Site Status

Countries

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Norway

References

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Skliarova T, Grawe RW, Vaag J, Mandahl A, Kolltveit I, Lovas I, Torgersen T, Lara-Cabrera ML. Pilot randomised controlled trial on the feasibility and intervention satisfaction with an educational group programme for adults with attention deficit hyperactivity disorder and their caregivers. BMC Psychiatry. 2025 Feb 20;25(1):161. doi: 10.1186/s12888-025-06570-4.

Reference Type DERIVED
PMID: 39979888 (View on PubMed)

Other Identifiers

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2017/2405 REK

Identifier Type: -

Identifier Source: org_study_id

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