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Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress (EAITDAS)

Primary Purpose

Depression, Anxiety, Stress

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Space from Depression
Space from Anxiety
Space from Stress
Sponsored by
Silver Cloud Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Depression, Anxiety, Stress, Online interventions, University students, CBT

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participants must be at least 18 years of age. Participants must have self-reported mild to severe symptoms of depression (5-27+) according to PHQ-9, self-reported mild to severe symptoms of anxiety (5-21+) according to GAD-7, or self-reported mild to severe symptoms of stress (15-34+) according to the stress sub-scale of DASS-21.

Exclusion Criteria:

  • Students who currently are in face-to-face therapy at UCCS or BHS will be excluded. Students who score in the "red zone" in terms of risk of self-harm on the screening questions routinely used at UCCS will not be referred to the study. Students who score greater than 0 on the PHQ-9 self-harm item during the initial screening phase will be automatically directed to be further evaluated and alerted that a counselor will try to reach them. Based on this further evaluation, they may be recommended to seek help from their health/counseling service and may/may not be eligible to participate in the study. They will be telephoned within 1 working day and contacted by email if they cannot be reached by phone.

Sites / Locations

  • University of Minnesota

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Depression Condition

Anxiety Condition

Stress Condition

Arm Description

Participants in this group will be offered the Space from Depression programme to be completed over an 8 week period. The programme is delivered through the online SilverCloud platform.

Participants in this group will be offered the Space from Anxiety programme to be completed over an 8 week period. The programme is delivered through the online SilverCloud platform.

Participants in this group will be offered the Space from Stress programme to be completed over an 8 week period. The programme is delivered through the online SilverCloud platform.

Outcomes

Primary Outcome Measures

Change in Stress sub-scale of Depression Anxiety and Stress Scale-21 (DASS-21)
Composed of 7-item sub-scale measuring symptoms of stress.
Change in Patient Health Questionnaire-9 (PHQ-9)
A self-report measure of depression that has been widely used in screening, primary care, and research.
Change in Generalized Anxiety Disorder-7 (GAD-7)
Comprises 7 items measuring symptoms and severity of GAD based on the DSM-IV diagnostic criteria for GAD.

Secondary Outcome Measures

Full Information

First Posted
November 19, 2015
Last Updated
September 7, 2018
Sponsor
Silver Cloud Health
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1. Study Identification

Unique Protocol Identification Number
NCT02614443
Brief Title
Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress
Acronym
EAITDAS
Official Title
Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress in University Students: Protocol for an Open Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
September 2017 (Actual)
Study Completion Date
September 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Silver Cloud Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aims of this study are to test the effectiveness and acceptability of internet-delivered treatment for depression, anxiety and stress in university students. These data will inform the methods for a future randomized controlled trial. The trial will establish an initial estimate of the effectiveness of these online interventions for students in terms of within-group effect sizes associated with changes in depression, anxiety and stress from pre to post-intervention and follow-up. These data will be used to estimate the sample size for a future trial to ensure that the study is sufficiently powered. A conservative estimate using the 90% upper confidence limit will be used to inform the sample size calculation of the definitive RCT. Acceptability of the intervention to participants will be assessed using data on usage and engagement with the intervention (e.g. percentage of participants completing each module, average number of log ins, average time spent per session and total time spent on the program). These data are acquired through the online SilverCloud system. Satisfaction with will be assessed through the use of a post-intervention questionnaire on satisfaction with accessing and using an online delivery format for treatment.
Detailed Description
Depression, anxiety and stress are among the primary causes of disease rates worldwide and are the most prevalent mental health problems in the U.S. Each is associated with significant economic, personal, intrapersonal and societal losses including lower quality of life and increased mortality. Depression, Anxiety and Stress in Students: Depression and anxiety are also the most prevalent mental health problems among the student population. In the 2010 American College Health Survey, 48% of college and university students reported feeling overwhelming anxiety at least once in the previous year. Thirty-one percent reported feeling so depressed it was difficult to function at least once in the previous 12 months. More recently, University counseling and mental health services have reported an increase in the number of clients seeking services and in yearly visits. The college years can be a highly stressful time in students' lives. This is particularly true of the period of transition to college as students are learning to cope with increased academic pressures. Students are at a developmental stage when newfound stressors can promote the onset of mental health difficulties. In addition to academic stress, international students can experience significant sociocultural adjustment demands. Young adults between 17 and 25 years of age are reported to be at greater risk of developing a serious mental illness than individuals in other age groups. Although early diagnosis of mental disorders can be difficult, delayed diagnosis can often lead to treatment resistance and poorer longer-term outcomes. In addition, underachievement or failure at this point in life can cause long-term setbacks to individuals' self-esteem and future progress. Treating Depression, Anxiety and Stress: Depression, anxiety and stress disorders can each be treated effectively using medications; however, after completing a course of this type of treatment the chances of relapse are high, and equally successful psychological therapies are often preferred. Of these, cognitive-behavior therapy (CBT) is the most widely researched and CBT is recognized as the leading choice of treatment for depression and anxiety in terms of post-treatment improvements, maintaining progress, and preventing relapse. CBT also is effective for stress management. CBT is comprised of a variety of cognitive and behavioral approaches, each concerned with changing distressing thoughts and beliefs. Treatment is often comprised of self-monitoring and thought recording, behavioral activation, cognitive restructuring, and exposure. Access to Treatment: On a global scale, a significant number of individuals in need of treatment receive no medical diagnosis nor do they seek treatment. The worldwide treatment gap between those needing treatment for depression compared to those receiving treatment has been estimated at 56%; the gap in treatment for anxiety disorders has been estimated at 46%. Several factors prevent people from accessing treatment, such as waiting lists, lack of motivation, negative attitudes about treatment, and costs. Of those willing to seek treatment, many encounter a lack of trained professionals or are placed on a waiting list. Although students can often obtain mental health services on campus, many campuses have limited services or have wait lists for services because of the high demand. A survey of U.S. students with mental health problems revealed that common barriers to seeking services, even if they were available, were stigma, lack of time/accessibility, and wait lists. Internet-delivered interventions are one way to address these issues. Internet-Delivered CBT (iCBT): Internet-delivered CBT programs are specially designed for the treatment of specific disorders, and can be either clinician-guided or self-administered. When such interventions are used in the UK, 6-8 sessions is the recommended length of treatment. Many studies provide support for the utility and effectiveness of internet-delivered treatments for depression, anxiety and stress . Those with the additional feature of human support tend to produce greater results. Several studies also have assessed the efficacy of online interventions for depression, stress, and anxiety for college students. Recent reviews of these studies have found evidence for the efficacy of these online interventions. However, most of these studies do not assess the efficacy of the interventions in the context of existing service delivery systems. Rather, many are RCTs assessing efficacy in convenience samples of students (e.g., Psychology majors). The current trial seeks to investigate the effectiveness and acceptability of internet-delivered interventions among university students seeking services and the procedures needed to incorporate these interventions into mental health delivery in U.S. universities. Additionally, it hopes to support and extend existing empirical evidence for SilverCloud programs. University of Minnesota: The University of Minnesota-Twin Cities is a public research university located in Minneapolis and St. Paul, Minnesota established in 1851. It is the oldest and largest campus within the University of Minnesota system and has the sixth-largest main campus student body in the United States, with 57,600 students. The university is organized into 19 colleges and schools. Participants will be recruited through three units at the University of Minnesota-Twin Cities. The first is Student Counseling Services (SCS) which provides free short-term counseling to undergraduate and graduate students. The second is Boynton Mental Health Clinic (BMHC) which also provides short term psychological services to full-time students at the University of Minnesota. Unlike SCS, BMHC also has psychiatrists on staff and is affiliated with the university health service. Finally, the investigators will recruit participants through the International Student and Scholar Services (ISSS) office which provides counseling to foreign national students on campus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Anxiety, Stress
Keywords
Depression, Anxiety, Stress, Online interventions, University students, CBT

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Depression Condition
Arm Type
Experimental
Arm Description
Participants in this group will be offered the Space from Depression programme to be completed over an 8 week period. The programme is delivered through the online SilverCloud platform.
Arm Title
Anxiety Condition
Arm Type
Experimental
Arm Description
Participants in this group will be offered the Space from Anxiety programme to be completed over an 8 week period. The programme is delivered through the online SilverCloud platform.
Arm Title
Stress Condition
Arm Type
Experimental
Arm Description
Participants in this group will be offered the Space from Stress programme to be completed over an 8 week period. The programme is delivered through the online SilverCloud platform.
Intervention Type
Other
Intervention Name(s)
Space from Depression
Intervention Description
Delivered through the online SilverCloud platform, the program for the treatment of depression employs several innovative engagement strategies for improving the user experience. These are divided into several categories: personal, interactive, supportive, and social.
Intervention Type
Other
Intervention Name(s)
Space from Anxiety
Intervention Description
Delivered through the online SilverCloud platform, the program for the treatment of anxiety employs several innovative engagement strategies for improving the user experience. These are divided into several categories: personal, interactive, supportive, and social.
Intervention Type
Other
Intervention Name(s)
Space from Stress
Intervention Description
Delivered through the online SilverCloud platform, the program for the treatment of stress employs several innovative engagement strategies for improving the user experience. These are divided into several categories: personal, interactive, supportive, and social.
Primary Outcome Measure Information:
Title
Change in Stress sub-scale of Depression Anxiety and Stress Scale-21 (DASS-21)
Description
Composed of 7-item sub-scale measuring symptoms of stress.
Time Frame
Baseline, postintervention at 8 weeks and 3 month follow-up
Title
Change in Patient Health Questionnaire-9 (PHQ-9)
Description
A self-report measure of depression that has been widely used in screening, primary care, and research.
Time Frame
Baseline, postintervention at 8 weeks and 3 month follow-up
Title
Change in Generalized Anxiety Disorder-7 (GAD-7)
Description
Comprises 7 items measuring symptoms and severity of GAD based on the DSM-IV diagnostic criteria for GAD.
Time Frame
Baseline, postintervention at 8 weeks and 3 month follow-up
Other Pre-specified Outcome Measures:
Title
Change in The Satisfaction with Treatment (SAT) Questionnaire
Description
Satisfaction measure containing two qualitative questions asking participants to describe what they most liked and least liked about the online treatment.
Time Frame
Postintervention at 8 weeks and 3 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants must be at least 18 years of age. Participants must have self-reported mild to severe symptoms of depression (5-27+) according to PHQ-9, self-reported mild to severe symptoms of anxiety (5-21+) according to GAD-7, or self-reported mild to severe symptoms of stress (15-34+) according to the stress sub-scale of DASS-21. Exclusion Criteria: Students who currently are in face-to-face therapy at UCCS or BHS will be excluded. Students who score in the "red zone" in terms of risk of self-harm on the screening questions routinely used at UCCS will not be referred to the study. Students who score greater than 0 on the PHQ-9 self-harm item during the initial screening phase will be automatically directed to be further evaluated and alerted that a counselor will try to reach them. Based on this further evaluation, they may be recommended to seek help from their health/counseling service and may/may not be eligible to participate in the study. They will be telephoned within 1 working day and contacted by email if they cannot be reached by phone.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Derek Richards, PhD
Organizational Affiliation
SilverCloud Health
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Patricia Frazier, PhD
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stefan G. Hofmann, PhD
Organizational Affiliation
Department of Psychological and Brain Sciences, Boston University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Deborah Beidel, PhD
Organizational Affiliation
UCF RESTORES, Department of Psychology, University of Central Florida
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patrick A. Palmieri, PhD
Organizational Affiliation
Center for the Treatment and Study of Traumatic Stress, Summa Health System, Akron, Ohio
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jacqueline Mooney, MA
Organizational Affiliation
SilverCloud Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christopher Bonner, MSc
Organizational Affiliation
SilverCloud Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-016-0068-9
Available IPD/Information Identifier
10.1186/s40814-016-0068-9

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Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress

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