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NCT Number: NCT04239729

Web-based Acceptance and Commitment Therapy for Hoarding Disorder

This study will help to determine if acceptance and commitment therapy delivered as a web-based intervention is a useful treatment for hoarding disorder and evaluate whether or not web-based treatment for hoarding is credible and acceptable. It may also help identify novel processes of change in hoarding treatment such as psychological inflexibility, mindfulness, and self-stigma.

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Key information

Conditions

Hoarding Disorder Anxiety Disorders Mental Disorders Obsessive-Compulsive Disorder

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Utah State University

Logan, Utah, 84322, United States

About this study

The efficacy of an ACT self-help website for hoarding will be assessed through a randomized, waitlist-controlled trial. Participants will be recruited from within the United States through a variety of channels. Given the need to recruit a targeted sample with clinical levels of hoarding symptoms, online advertisements through Facebook and Google AdWords will be the primary recruitment method. Participants will complete an initial brief screening, provide consent, and then complete a baseline survey. Each of these steps will be completed online and participants will be automatically guided from each step to the next. That is, those who screen as eligible will be automatically directed to an online consent form, and those who provide consent will be automatically directed to begin the initial online baseline survey. They will be randomly assigned automatically upon completing the baseline survey to either use the ACT self-help website and receive supportive coaching for the next 8 weeks, or wait for the next 8 weeks. After 8 weeks, participants will be asked to complete a posttreatment survey. They will be asked to complete a final, follow-up survey after an additional 4 weeks after the posttreatment survey. After the follow-up survey is completed, waitlisted participants will be provided with access to the website. The website will implement a self-help version of ACT. Participants will be asked to complete 16 brief self-help website sessions, each taking around 15-20 minutes to finish, twice a week for eight weeks. Participants assigned to the website condition will also receive coaching.The purpose of coaching will be to help participants engage with the website and adhere to the intervention. Coaching will consist of an initial phone call of 10-15 minutes followed by weekly email contact during the 8-week treatment period. Coaches will be graduate students trained in clinical psychology.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years old or older
  • Living in the USA
  • Seeking help for clutter and/or hoarding
  • Interested in testing a self-help website
  • Scoring at or above the clinical cutoff of 41 on the Saving Inventory-Revised

Exclusion criteria

  • 17 years or younger
  • Living outside the USA
  • Not seeking help for clutter and/or hoarding
  • Not interested in testing a self-help website
  • Scoring below 41 on the Saving Inventory-Revised

Treatment and study plan

ACT Website and Coaching

Behavioral

The ACT website includes sixteen sessions and is designed to teach a series of skills from ACT applied to hoarding. The intervention also includes brief supportive coaching (an initial phone call and weekly support over email).

Primary outcomes

  1. Saving Inventory-Revised (SI-R; Frost et al., 2004)

    Time frame: Posttreatment (8 weeks after baseline)

    A self-report measure of hoarding symptoms

Secondary outcomes

  1. Sheehan Disability Scale (Sheehan, Harnett-Sheehan, & Raj, 1996)

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    A self-report measure of functional impairment due to symptoms. Higher scores indicate greater impairment. Scores range from 0 to 30.

  2. Clinical Global Impression - Improvement (CGI-I; Guy, 1976).

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    A self-report measure of overall improvement in symptoms

  3. General Health Questionnaire-12 (GHQ-12; Goldberg, 1978)

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    A self-report measure of overall psychological distress

  4. Stigma of hoarding items (Chasson et al., 2018)

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    Seven self-report items assessing stigma towards individuals with hoarding disorder. These items are not a standardized scale but have been used in previous research (Chasson et al., 2018). Three items assess perceived difference (Example: How like or unlike do you think is a person with obsessive-compulsive disorder compared to everyone else in the general population?), three items assess disdain (Example: How good or bad do you think is a person with hoarding disorder compared to everyone else in the general population?) and one item assesses blame: How responsible do you think a person with serious mental illness is for his or her condition?

  5. Acceptance and Action Questionnaire for Hoarding (AAQH; Krafft et al., in press)

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    A self-report measure of hoarding-related psychological inflexibility

  6. Five-Facet Mindfulness Questionnaire - Acting with Awareness (FFMQ-AA; Baer, Smith, Hopkins, Krietemeyer, & Toney, 2006)

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    A self-report measure of the acting with awareness facet of mindfulness

  7. Valuing Questionnaire-Progress (VQ-Progress; Smout, Davies, Burns, & Christie, 2014)

    Time frame: Posttreatment (8 weeks after baseline) and follow-up (12 weeks after baseline)

    A self-report measure of progress toward personal values

  8. Credibility/Expectancy Questionnaire (CEQ; Devilly & Borkovec, 2000).

    Time frame: After using first website session (approximately 0-1 weeks after baseline)

    A self-report measure of the perceived credibility of and expectations toward a treatment. Only administered to treatment condition

  9. System Usability Scale (Tullis & Albert, 2008)

    Time frame: Posttreatment (8 weeks after baseline)

    A self-report measure of usability of a technological system. Only administered to treatment condition. High scores indicated greater usability, and scores range from 0 to 100.

  10. Treatment Evaluation Inventory-Short Form (TEI-SF; Kelley, Heffer, Gresham, & Elliott, 1989).

    Time frame: Posttreatment (8 weeks after baseline)

    A self-report measure of treatment acceptability. Only administered to treatment condition

  11. Novel satisfaction item 1

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "Overall, I was satisfied with the quality of the program." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  12. Novel satisfaction item 2

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "The program was helpful to me." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  13. Novel satisfaction item 3

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "The program was easy to use." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  14. Novel satisfaction item 4

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "I felt the program was made for someone like me." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  15. Novel satisfaction item 5

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "I would recommend the program to other people with a clutter and/or hoarding problem." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  16. Novel satisfaction item 6

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "The psychological skills taught (ex. mindfulness, opening up) were helpful to me." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  17. Novel satisfaction item 7

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "The practice exercises (ex. discarding, goal setting) were helpful to me." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  18. Novel satisfaction item 8

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "This treatment fit well with my goals." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  19. Novel satisfaction item 9

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "Overall, I was satisfied with the coaching that I received." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  20. Novel satisfaction item 10

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked to rate agreement from 1 (Strongly disagree) to 6 (Strongly agree) with the statement "The website would have been just as useful without a coach." This is a novel satisfaction item specific to this study. Only administered to treatment condition

  21. Novel satisfaction item 11

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked an open-ended question to gather qualitative feedback on the intervention. Only assigned to treatment condition. The question is, "What did you like best about the Making Space program?"

  22. Novel satisfaction item 12

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked an open-ended question to gather qualitative feedback on the intervention. Only assigned to treatment condition. The question is, "What was the most important thing you learned from the Making Space program?"

  23. Novel satisfaction item 13

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked an open-ended question to gather qualitative feedback on the intervention. Only assigned to treatment condition. The question is, "What did you like least about the Making Space Program? Why did you like this the least?"

  24. Novel satisfaction item 14

    Time frame: Posttreatment (8 weeks after baseline)

    Participants will be asked an open-ended question to gather qualitative feedback on the intervention. Only assigned to treatment condition. The question is, "Do you have any other comments or suggestions regarding our Making Space program?"

Sponsors and collaborators

Lead sponsor

Utah State University

Other

Registry information

Official study title

A Randomized Waitlist-controlled Trial of Web-based Acceptance and Commitment Therapy for Hoarding Disorder

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jan 27, 2020
Registry last updated
Apr 27, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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