Internet-based Support for Young People With ADHD and Autism - a Controlled Study

Sponsor
Göteborg University (Other)
Overall Status
Completed
CT.gov ID
NCT02300597
Collaborator
Södra Älvsborg Hospital (Other), Habilitation Services in Skaraborg, Skövde (Other)
45
1
2
57
0.8

Study Details

Study Description

Brief Summary

Young people between age 15 and 25 with ADHD and/or autism spectrum disorders are offered internet-based support and coaching during eight weeks (chat and e-mail). Data is collected before and after the intervention and six months after end of treatment using self-report questionnaires pertaining to sense of coherence, self-esteem, quality of life, depressive and anxiety symptoms and socioeconomic status. Parents complete an assessment scale for the next of kin. After treatment the young people are interviewed regarding the quality of the intervention. A comparison group matched for age, gender and neuropsychiatric diagnosis is offered treatment as usual and is assessed at the same time points as the intervention group. The individuals are not randomized due to difficulties to recruit if the individuals do not know group assignment in advance.

Condition or Disease Intervention/Treatment Phase
  • Other: Internet based support and coaching
N/A

Detailed Description

Young people between age 15 and 25 with ADHD and/or autism spectrum disorders are consecutively included in the project and are offered coaching and support during eight weeks over the internet (chat and e-mail) twice a week. Data is collected before and after the intervention as well as six months after end of treatment using self-report questionnaires (Sense of Coherence (SOC), Rosenberg Self Esteem Scale, Manchester Short Assessment of Quality of Life (MANSA), Montgomery Asberg Depression Rating Scale (MADRS), and Hospital Anxiety and Depression Scale (HAD)). A parent or a partner completes an assessment scale for the next of kin. When treatment is completed, the young people are interviewed using a structured interview pertaining to the quality of the intervention. A comparison group matched for age, gender and neuropsychiatric diagnosis is offered treatment as usual (TAU) and is assessed at the same time points as the intervention group. The individuals are not randomized to the intervention and comparison groups due to difficulties to recruit if the individuals do not know group assignment in advance. In all, 24 individuals will be offered the intervention and 24 individuals will receive TAU.

Study Design

Study Type:
Interventional
Actual Enrollment :
45 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Internet-based Support and Coaching for Adolescents and Young Adults With ADHD and Autism Spectrum Disorders - a Controlled Study
Study Start Date :
Sep 1, 2010
Actual Primary Completion Date :
Jun 1, 2015
Actual Study Completion Date :
Jun 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Internet based support and coaching

Young people between age 15 and 25 with ADHD and/or autism spectrum disorders are offered internet-based support and coaching during eight weeks (chat and e-mail). Data is collected before and after the intervention and six months after end of treatment using self-report questionnaires pertaining to sense of coherence, self-esteem, quality of life, depressive and anxiety symptoms and socioeconomic status. Parents complete an assessment scale for the next of kin. After treatment the young people are interviewed regarding the quality of the intervention.

Other: Internet based support and coaching
Young people between age 15 and 25 with ADHD and/or autism spectrum disorders are offered internet-based support and coaching during eight weeks (chat and e-mail). Data is collected before and after the intervention and six months after end of treatment using self-report questionnaires pertaining to sense of coherence, self-esteem, quality of life, depressive and anxiety symptoms and socioeconomic status. Parents complete an assessment scale for the next of kin. After treatment the young people are interviewed regarding the quality of the intervention.

No Intervention: Treatment as usual (TAU)

A comparison group matched for age, gender and neuropsychiatric diagnosis is offered treatment as usual and is assessed at the same time points as the intervention group.

Outcome Measures

Primary Outcome Measures

  1. QoL [T2: immediately after intervention; T3: 6 months after intervention. Outcome Measure is going to report a change.]

    Self report questionnaire; Manchester Short Assesment of Quality of Life (MANSA), Priebe et. al. 1999.

Secondary Outcome Measures

  1. Self esteem [T2: immediately after intervention; T3: 6 months after intervention]

    Self report questionnaire; Rosenberg Self-Esteem Scale (Rosenberg, 1965, 1989)

  2. Sense of coherence [T2: immediately after intervention; T3: 6 months after intervention]

    Self report questionnaire; Sense of Coherence (SOC-29), Antonovsky, 1987.

  3. Anxiety and depressive symptoms [T2: immediately after intervention; T3: 6 months after intervention]

    Self report questionnaire; Hospital Anxiety and Depression Scale (HAD), Zigmond & Snaith, 1983.

  4. Depressive symptoms [T2: immediately after intervention; T3: 6 months after intervention]

    Self report questionnaire; Montgomery Asberg Depression Rating Scale (MADRS), Montgomery & Asberg, 1979.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ADHD and/or autism spectrum disorder

  • Age 15 to 30

Exclusion Criteria:
  • No current antisocial behaviour, psychotic symptoms and/or alcohol/substance abuse

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Psychiatry and Neurochemistry, Institute of Neurosceince and Physiology Gothenburg Sweden SE-413 45

Sponsors and Collaborators

  • Göteborg University
  • Södra Älvsborg Hospital
  • Habilitation Services in Skaraborg, Skövde

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elisabet Wentz, Associate professor, Göteborg University
ClinicalTrials.gov Identifier:
NCT02300597
Other Study ID Numbers:
  • IBSC-2
First Posted:
Nov 25, 2014
Last Update Posted:
May 21, 2019
Last Verified:
May 1, 2019
Keywords provided by Elisabet Wentz, Associate professor, Göteborg University
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 21, 2019