NCT01296321

Brief Summary

The purpose of this study is to determine whether tailored internet-administrated CBT is a feasible approach in the treatment of panic symptoms and comorbid anxiety and depressive symptoms.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
57

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2010

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2010

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

February 14, 2011

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 15, 2011

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2011

Completed
Last Updated

February 16, 2011

Status Verified

February 1, 2011

Enrollment Period

1.2 years

First QC Date

February 14, 2011

Last Update Submit

February 15, 2011

Conditions

Outcome Measures

Primary Outcomes (1)

  • Panic Disorder Severity Scale (PDSS)

    Change from baseline in panic symptoms two weeks post treatment, at six months and at 12 months post treatment.

    Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Secondary Outcomes (4)

  • Clinical Outcome in Routine Evaluation - Outcome Measure (CORE-OM)

    Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

  • Beck Anxiety Inventory (BAI)

    Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

  • Montgomery Åsberg Depression Rating Scale-Self Rated (MADRS-S)

    Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

  • Quality of Life Inventory (QOLI)

    Two weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Study Arms (2)

Tailored Internet-delivered CBT

EXPERIMENTAL

Behavioral: Tailored Internet-delivered CBT

Behavioral: Tailored Internet-administrated CBT-Treatment

Waitlist

ACTIVE COMPARATOR

Waitlist.

Behavioral: Waitlist

Interventions

This intervention contains 6-8 text-based self-help modules in which 4 modules are fixed (the first three and the last) and the rest are "prescribed following the diagnostic telephone interview. These modules contain material on panic disorder, social phobia, stress management, assertiveness training, concentration, relaxation among other things.

Tailored Internet-delivered CBT
WaitlistBEHAVIORAL

Passive waitlist during 8-10 weeks.

Waitlist

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Be between the ages of 18-30 years old or 31-46 years old
  • Have reoccurring panic attacks

You may not qualify if:

  • Suicide prone
  • Alcohol addiction
  • PTSD
  • OCD
  • Ongoing psychological treatment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Silfvernagel K, Carlbring P, Kabo J, Edstrom S, Eriksson J, Manson L, Andersson G. Individually tailored internet-based treatment for young adults and adults with panic attacks: randomized controlled trial. J Med Internet Res. 2012 Jun 26;14(3):e65. doi: 10.2196/jmir.1853.

MeSH Terms

Conditions

Anxiety DisordersDepression

Interventions

Waiting Lists

Condition Hierarchy (Ancestors)

Mental DisordersBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Appointments and SchedulesOrganization and AdministrationHealth Services Administration

Study Officials

  • Gerhard Andersson, PhD

    Department of Behavioral Sciences and Learning, Linköping University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

February 14, 2011

First Posted

February 15, 2011

Study Start

February 1, 2010

Primary Completion

April 1, 2011

Study Completion

April 1, 2011

Last Updated

February 16, 2011

Record last verified: 2011-02