- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03807154
Guided Online Self-help for Loneliness
SOLUS - A Randomized Controlled Two-site Trial Comparing Internet-based Cognitive Behavioral Therapy and Internet-based Interpersonal Psychotherapy
The study seeks to investigate the efficacy of two internet-based self-help programmes administered with support from a therapist. The two active conditions consist of an internet cognitive behavioral therapy (ICBT) programme and a intervention of internet-based interpersonal psychotherapy (IIPT), both of which have been developed for the present study. The active conditions will be compared to a wait-list control group.
Participants will be recruited in Sweden with a nationwide recruitment.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Östergötland
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Linköping, Östergötland, Sweden, 58183
- Department of Behavioral Sciences and Learning, Linköping University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Frequent and distressing experiences of loneliness
- Can speak, write, and read the primary language of the country in which they reside (Sweden or the United Kingdom).
- Have access to an internet connection and a computer/smart phone/tablet
- Are prepared to participate in the study, regardless of the type of treatment they are randomly assigned to.
Exclusion Criteria:
- Changes in dosage of psychopharmaceutic medication in the last three months prior to the start of the study or a planned change during the initial treatment period.
- Other ongoing psychotherapeutic treatment
- Suicidal plans
- A previously diagnosed personality syndrome
- Ongoing substance abuse
- Other acute treatment need related to a psychiatric disorder requiring attention from a mental health professional (e.g. eating disorders such as anorexia nervosa).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Internet-based cognitive behavioral therapy (ICBT)
A nine-week long ICBT intervention with therapist support.
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A nine week long ICBT-programme with therapist guidance.
Based on cognitive and behavioral techniques that have been tailored to address loneliness.
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Experimental: Internet-based Interpersonal Therapy (IIPT)
A nine-week long intervention based in interpersonal psychotherapy with therapist support.
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A nine week long internet-based IPT-programme with therapist guidance.
Contains three distinct phases: assessment phase (three weeks), focus phase (five weeks, during which the participants will choose from one of four primary problem areas during the three latter weeks), and end phase (one week).
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No Intervention: Wait-list
Wait-list control group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change on UCLA Loneliness Scale, Version 3 (UCLA-LS-3)
Time Frame: During week 2, 4, 6, and 8 of the intervention, 10 weeks after start of intervention, 4 months after completion of intervention, 12 months after start of intervention.
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Measure of loneliness, total score ranging from 20-80 (representing the sum of each of the 20 individual items).
Lower scores represent less loneliness and a more favourable outcome.
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During week 2, 4, 6, and 8 of the intervention, 10 weeks after start of intervention, 4 months after completion of intervention, 12 months after start of intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change on Brunnsviken Brief Quality of Life Scale (BBQ)
Time Frame: 10 weeks after start of intervention, at 4 month follow-up, 12 month follow-up
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Measure of quality of life, total score ranging from 0 to 96 with a higher score indicating a higher quality of life.
The scores of each of the six primary questions regarding perceived quality of life within an area of life are multiplied with the score of an item measuring the perceived importance of the area in question.
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10 weeks after start of intervention, at 4 month follow-up, 12 month follow-up
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Change on Patient Health Questionnaire (PHQ-9)
Time Frame: 10 weeks after start of intervention, at 4 month follow-up, at 12 month follow-up
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Measure of depressive symptoms.
Possible range for the total sum: 0 to 27 (created by summing up the score from each item).
Clinical cut-offs for mild, moderate, moderately severe and severe major depressive disorder are considered to be 5, 10, 15, and 20 points.
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10 weeks after start of intervention, at 4 month follow-up, at 12 month follow-up
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Change on Social Interaction Anxiety Scale (SIAS)
Time Frame: 10 weeks after start of intervention, at 4 month follow-up, at 12 month follow-up
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Measure of social interaction anxiety, closely correlated with social anxiety disorder.
The score on each of the 20 items are summed up.
Possible range for the total sum between 0 and 80. Higher scores indicate a higher degree of social interaction anxiety.
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10 weeks after start of intervention, at 4 month follow-up, at 12 month follow-up
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Change on Generalised Anxiety Disorder 7-item scale (GAD-7)
Time Frame: 10 weeks after start of intervention, at 4 month follow-up, at 12 month follow-up
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Measure of symptoms of generalised anxiety disorder (GAD).
Seven items, the score is interpreted by summing up the score from each individual item.
Higher scores indicate more severe problems with worry and generalised anxiety.
The total sum ranges from 0 to 21 with cut-offs of 5, 10, and 15 representing mild, moderate and severe generalised anxiety.
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10 weeks after start of intervention, at 4 month follow-up, at 12 month follow-up
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Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SOLUS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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