ClinicalTrials.gg
CompletedNCT02584764Updated Aug 18, 2017

Internet Supported Group Cognitive Behavior Therapy (CBT) for Hoarding Disorder (HD)

An interventional study of Cognitive behavior therapy and Internet support in Hoarding Disorder, sponsored by Karolinska Institutet. Completed at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-08-18.

Sponsored by Karolinska Institutet · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The primary aim is to develop, and test the feasibility and efficacy of, a manual based, cognitive behaviour therapy (CBT) treatment for Hoarding Disorder (HD) delivered in a group format combined with an Internet support system. The investigators' secondary aim is to investigate the neurocognitive profile of the participants before and after treatment in order to explore if the treatment might have an impact on neurocognitive functioning and if certain neurocognitive profiles predict outcome.

For the primary aim, the investigators hypothesize that the treatment will be acceptable to participants and decrease symptoms of hoarding. Regarding the secondary aim, the investigators hypothesize that deficiencies in executive functioning, as measured with a neurocognitive battery, will reduce upon completion of treatment and that baseline executive function will be associated with treatment outcome.

02

Conditions studied

  • Hoarding Disorder

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03

In context

Hoarding Disorder

32 studies on the registry are indexed under Hoarding Disorder; 5 are open to participants now.

This study's enrollment of 20 is below the median of 37 across 28 interventional studies indexed under Hoarding Disorder.

Browse Hoarding Disorder studies →

Lead sponsor

Karolinska Institutet is the lead sponsor of 1,148 studies on the registry; 276 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Outpatients

    • Male or female
    • ≥ 18 years of age
    • Currently living in Stockholm county
    • Primary diagnosis of Hoarding Disorder according to
    • Signed
    • Regular access to a computer with Internet and ability to use Internet
    • Access to a mobile phone
    • Able to participate in group sessions

Exclusion criteria

  • Current substance dependence or misuse

    • Life time bipolar disorder or psychosis
    • Severe self-rated depressive symptoms (score ≥ 35 on MADRS-S)
    • Suicidal ideation (score > 4 on item 9 in MADRS-S)
    • Psychotropic medication changes within two months prior to the treatment
    • Other current psychological treatment that could affect hoarding symptoms
    • Has received more than 10 CBT sessions for Hoarding Disorder
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    CBT with Internet support

    16 sessions of Cognitive behavior therapy in group with Internet support between group sessions

    Behavioral: Cognitive behavior therapy · Behavioral: Internet support

Interventions

  • BehavioralCognitive behavior therapy

    Also known as: CBT

  • BehavioralInternet support
06

What researchers measure

Primary outcomes

  1. Saving Inventory - Revised (SI-R)

    The SI-R is a 23-item self-report questionnaire. It assesses hoarding symptoms in 3 sub-scales: difficulty discarding, clutter and excessive acquisition.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

Secondary outcomes

  1. Hoarding Rating Scale - Self Report (HRS-SR)

    A 5-item self-report questionnaire assessing hoarding symptoms.

    Time frame: Weekly change during treatment, weeks 1-15

  2. Saving Cognitions Inventory (SCI)

    The questionnaire is a 24-item self-report questionnaire assessing beliefs and attitudes participants experience when trying to discard items. It is divided in 4 subscales:emotional attachment to objects, beliefs about objects as memory aids, responsibility for not wasting possessions, and the need for control over possessions.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  3. Clutter Image Rating (CIR)

    This scale consists of three sets of photographs each containing nine photos of a single room with varying levels of clutter. Study participants will select the photograph that best resembles his or her own home. The study investigators will also conduct blinded ratings of the same photos.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  4. Global Assessment of Functioning (GAF)

    A scale used to rate the social, occupational, and psychological functioning of the study participants.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  5. Clinical global impression (CGI)

    A 7 point scale to rate how much the patient's illness has improved or worsened relative to a baseline state at the beginning of the intervention.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  6. EuroQol- 5 Dimension (EQ-5D)

    A self-rating scale assessing quality of life i 5 dimensions.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  7. Trimbos and Institute of Medical Technology Assessment Cost Questionnaire for Psychiatry (TIC-P)

    In this questionnaire, study participants register their monthly health care consumption (e.g. GP visits) as well as time spent in informal health enhancing activities (e.g. self-help groups and informal care from friends). Additionally, work loss and work cutback both at work and in the domestic realm is measured.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

Other outcomes

  1. Hoarding disorder diagnosis

    Presence of Hoarding Disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). Assessed by the investigators using the Structured Interview for Hoarding Disorder.

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  2. Comorbid psychiatric diagnoses

    Presence of psychiatric diagnoses other than Hoarding Disorder. Assessed by the investigators using the M.I.N.I. International Neuropsychiatric Interview (M.I.N.I. 6.0).

    Time frame: Change from baseline to treatment week 8,16, 3- and 12-month follow-up

  3. Neuropsychological Test Battery (CANTAB)

    Cambridge Automated Neuropsychological Test Battery (CANTAB) will be used to test the study participants in 3 aspects of executive function: shifting and flexibility of attention, visuospatial working memory and response inhibition

    Time frame: Change from baseline to treatment week 16

  4. Client Satisfaction Questionnaire - 8 (CSQ-8)

    An 8-item questionnaire measuring treatment satisfaction and acceptability.

    Time frame: At treatment week 16

  5. Homework adherence

    Self-reported time spent on homework each week.

    Time frame: Weekly change during treatment, weeks 1-15

07

Study locations

1 site
  • Psykiatri Nordväst, Stockholms Läns Sjukvårdsområde (SLSO), Stockholms Läns Landsting
    Stockholm, Sweden
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Oct 2015 to primary completion in Jun 2017, 20 months.

Of 20 interventional studies with no phase under Hoarding Disorder, half reached primary completion within 33 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 48. This study's 20 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 13, 2015
First posted
Oct 23, 2015
StartActual
Oct 2015
Primary completionActual
Jun 2017
CompletionActual
Jun 2017
Last update
Aug 18, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 18, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02584764
Responsible party
Christian Rück (Associate Professor, Karolinska Institutet) — Principal investigator
First posted
Oct 23, 2015
Start date
Oct 2015
Primary completion
Jun 2017
Completion
Jun 2017
Last update
Aug 18, 2017

Study contacts

Christian Rück, Assoc Prof
principal investigator · Karolinska Institutet

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2017. You cannot join it, but the record below documents what was studied.

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