Internet-based Self-help Treatment for Panic Disorder: Two Ways of Complementary Psychological Support

Sponsor
Universitat Autonoma de Barcelona (Other)
Overall Status
Completed
CT.gov ID
NCT02402322
Collaborator
(none)
77
3
15

Study Details

Study Description

Brief Summary

The aim of this study was to compare two ways of administrating the complementary psychological support (scheduled vs. non-scheduled) in an online self-help program for panic disorder. In order to do so, the investigators studied: a) If there were differences in the intensity and frequency of the symptoms of panic disorder. b) If there were differences in the therapeutic adherence between the subjects receiving both kinds of complementary support.

  1. If the more time spent by a psychologist in therapeutic interventions produced the best results of therapeutic adherence / symptom improvement.

Seventy seven subjects followed the online self-help program for 8 weeks; 27 subjects had the support of a therapist via phone when they required it, 25 subjects had the support of a therapist weekly and 25 subjects were in the waiting list as a control group.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Scheduled support
  • Behavioral: Non-scheduled support
N/A

Detailed Description

The aim of this study was to compare two ways of administrating the complementary psychological support (scheduled vs. non-scheduled) in an online self-help program for panic disorder. In order to do so, the investigators studied: a) If there were differences in the intensity and frequency of the symptoms of panic disorder. b) If there were differences in the therapeutic adherence between the subjects receiving both kinds of complementary support.

  1. If the more time spent by a psychologist in therapeutic interventions produced the best results of therapeutic adherence / symptom improvement.

Treatment program

Internet-based self-help program for anxiety disorders "FREE OF ANXIETY" was developed, based on cognitive behavioral therapy. The program is presented as an interactive course, which is divided into eight weekly modules.A number of therapeutic components are used: psychological education (modules 1-8), behavioral analysis (safety and avoidance behavior) (module 2), in vivo and interoceptive exposure (modules 2-8), relaxation training and diaphragmatic breathing (modules 1-4), cognitive restructuring (modules 4-5), mindfulness (Module 6) communication training (module 7), problem solving Module 8). The program also includes a messaging system between therapists and subjects.

Participants and Procedure

The participants were recruited using a google banner linked to searches about anxiety disorders. The individuals were redirected to a Web page which contained information about anxiety disorders and the aims of the study. Suicide risk (score of 3 in the 15th item of the Web Screening Questionnaire) was established as an exclusion criterion. The study was approved by the ethics committee of the Autonomous University of Barcelona.

Applicants completed the informed consent, the demographic questionnaire and a screening questionnaire online. One week later a psychologist who had been trained to apply the MINI International Neuropsychiatric Interview (Sheehan, Lecrubier, Harnett-Sheehan, Janavs,Weiller, Bonora, et al., 1997) assessed the presence of a current psychiatric diagnosis. Participants with Panic Disorder completed a battery of self-reported measures in order to assess panic disorder, anxiety, and depression symptoms.

After clinical evaluation, the participants were divided into three groups by a true random-number service.

The data collected were anonymized and coded

Seventy seven subjects followed the online self-help program for 8 weeks; 27 subjects had the support of a therapist via phone when they required it, 25 subjects had the support of a therapist weekly and 25 subjects were in the waiting list as a control group.

Participants completed self-reported measures at the end of the treatment, and six months later.

Statistical analyses

The investigators studied differences between participants with and without Panic Disorder regarding their gender and age, using Chi-square test and Student t-test.

The participants' pretreatment and posttreatment measures were analyzed with analysis of variance (ANOVA) with repeated measures. These were followed by t tests with Bonferroni-corrected p values. Effect sizes were calculated both within and between groups, and all calculations were based on the pooled standard deviation, Cohen's d.

All analyses were conducted using SPSS version 22 for Windows.

Study Design

Study Type:
Interventional
Actual Enrollment :
77 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Internet-based Self-help Treatment for Panic Disorder: A Randomised Controlled Trial of Two Ways of Administrating the Complementary Psychological Support (Scheduled vs. Non-scheduled)
Study Start Date :
Aug 1, 2013
Actual Primary Completion Date :
Nov 1, 2014
Actual Study Completion Date :
Nov 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Non-scheduled support

Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it.

Behavioral: Non-scheduled support
Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it.

Experimental: Scheduled support

Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly.

Behavioral: Scheduled support
Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly.

No Intervention: Waiting list

Participants in a waiting list.

Outcome Measures

Primary Outcome Measures

  1. Change From Baseline Score in the Panic Disorder Severity Scale at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    Panic Disorder Severity Scale Self-Report (PDSS-SR). This 7-item scale assesses the severity of PD through questions about the frequency of panic attacks, associated distress, anticipatory anxiety, agoraphobic and interoceptive avoidance, and social and work impairment. Score range: 0-28. Scores up to 10 correspond with ''mild,'' those between 11 and 15 with ''moderate,'' and those at or above 16 with ''severe'' panic disorder.

  2. Change From Baseline Score in the Anxiety Sensitivity Index-3 at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    This 18-item scale evaluates sensitivity to anxiety symptoms on 3 dimensions: physical, cognitive, and social.There are 3 subscales, physical, cognitive, and social. For both the subscales (which range from 0 to 24) and the total scale (which range from 0 to 72), higher scores correspond to greater anxiety sensitivity.

Secondary Outcome Measures

  1. Change From Baseline Score in the Beck Anxiety Inventory at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    Beck Anxiety Inventory (BAI), Spanish adaptation . This 21-item self-reported instrument evaluates the cognitive and physical symptoms of anxiety. Score range:0- 63, with 3 levels of severity 0-21 mild anxiety, 22-35 moderate anxiety and 36-63 severe anxiety.

  2. Change From Baseline Score in the Beck Depression Inventory at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    Beck Depression Inventory-II (BDI-II), Spanish adaptation (38, 39). This 21-item self-reported instrument evaluates symptoms of depression. Score range:0- 63, with 3 levels of severity, 10-18 mild depression, 19-29 moderate depression and >30 severe depression.

  3. Change From Baseline Score in the Sheehan Disability Inventory (Work Subscale) at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.

  4. Change From Baseline Score in the Sheehan Disability Inventory (Social Life Subscale) at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.

  5. Change From Baseline Score in the Sheehan Disability Inventory (Family Subscale) at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.

  6. Change From Baseline Score in the Sheehan Disability Inventory (Stress Subscale) at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.

  7. Change From Baseline Score in the Sheehan Disability Inventory (Social Support Subscale) at 8 Weeks and 6 Months. [Baseline, 8 weeks, 6 months.]

    This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Meet Diagnostic Statistical Manual criteria for panic disorder.

  • Have suffered from panic disorder at least one year.

  • Suffer from panic disorder as primary pathology.

  • If the participant was taking medication for panic disorder / agoraphobia, the dose should be stable three months before the start of the program.

Exclusion Criteria:
  • Obtain a score of 26 or more on the Beck Depression Inventory II

  • Suffer from another psychiatric illness that requires immediate attention.

  • Risk of suicide, indicated by a score of 3 on the screening questionnaire.

  • Being or having been in cognitive behavioral therapy .

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Universitat Autonoma de Barcelona

Investigators

  • Study Director: Beatriz Molinuevo, PhD, Department of Psychiatry and Forensic Medicine, Institute of Neurosciences, School of Medicine, Universitat Autònoma de Barcelona, Spain

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pablo Oromendia, PhD Candidate, Universitat Autonoma de Barcelona
ClinicalTrials.gov Identifier:
NCT02402322
Other Study ID Numbers:
  • PTCCAP
First Posted:
Mar 30, 2015
Last Update Posted:
Dec 7, 2015
Last Verified:
Oct 1, 2015
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details Participants were recruited through advertisements on the Internet and were redirected to a website containing information about the study. Individuals interested in taking part in the study completed a screening questionnaire and provided demographic data. Participants were recruited between August, 2013 and February 2014.
Pre-assignment Detail Individuals were evaluated thoroughly using the MINI International Neuropsychiatric Interview. One hundred and twenty-five individuals were assessed and 48 were excluded from the trial because they suffered from another disorder (n=34), their medication was not stable (n = 13), or they had received Cognitive Behavioral Therapy (n = 1).
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Period Title: Pretreatment
STARTED 27 25 25
Posttreatment Measures 24 24 24
COMPLETED 24 24 24
NOT COMPLETED 3 1 1
Period Title: Pretreatment
STARTED 24 24 24
COMPLETED 18 21 0
NOT COMPLETED 6 3 24

Baseline Characteristics

Arm/Group Title Non-scheduled Support Scheduled Support Waiting List Total
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list. Total of all reporting groups
Overall Participants 27 25 25 77
Age (years) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [years]
39.4
(8.5)
38.2
(7.8)
44.6
(10.3)
40.7
(9.3)
Sex: Female, Male (Count of Participants)
Female
19
70.4%
19
76%
15
60%
53
68.8%
Male
8
29.6%
6
24%
10
40%
24
31.2%
Region of Enrollment (participants) [Number]
Spain
27
100%
25
100%
25
100%
77
100%

Outcome Measures

1. Primary Outcome
Title Change From Baseline Score in the Panic Disorder Severity Scale at 8 Weeks and 6 Months.
Description Panic Disorder Severity Scale Self-Report (PDSS-SR). This 7-item scale assesses the severity of PD through questions about the frequency of panic attacks, associated distress, anticipatory anxiety, agoraphobic and interoceptive avoidance, and social and work impairment. Score range: 0-28. Scores up to 10 correspond with ''mild,'' those between 11 and 15 with ''moderate,'' and those at or above 16 with ''severe'' panic disorder.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
15.29
(4.21)
15.75
(4.52)
13.08
(3.81)
8 weeks
10.42
(3.14)
7.21
(2.16)
13.13
(4.5)
Six months
10.21
(2.57)
8.33
(2.61)
13.13
(4.5)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Non-scheduled Support, Scheduled Support, Waiting List
Comments The participants' pre- and posttreatment scores were studied with repeated measures ANOVA. Within- and between-group effect sizes were calculated using the pooled standard deviation, Cohen's d.
Type of Statistical Test Non-Inferiority or Equivalence
Comments In the preliminary analysis, we studied the possible group differences in demographic data and pretreatment measures with chi-square tests and analysis of variance (ANOVA).
Statistical Test of Hypothesis p-Value 0.05
Comments
Method ANOVA
Comments
2. Primary Outcome
Title Change From Baseline Score in the Anxiety Sensitivity Index-3 at 8 Weeks and 6 Months.
Description This 18-item scale evaluates sensitivity to anxiety symptoms on 3 dimensions: physical, cognitive, and social.There are 3 subscales, physical, cognitive, and social. For both the subscales (which range from 0 to 24) and the total scale (which range from 0 to 72), higher scores correspond to greater anxiety sensitivity.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
31.04
(10.13)
29.00
(9.7)
26.83
(11.56)
8 weeks
21.54
(10.07)
14.75
(7.71)
28.08
(11.94)
6 months
22.17
(9.86)
16.13
(9.82)
28.08
(11.94)
3. Secondary Outcome
Title Change From Baseline Score in the Beck Anxiety Inventory at 8 Weeks and 6 Months.
Description Beck Anxiety Inventory (BAI), Spanish adaptation . This 21-item self-reported instrument evaluates the cognitive and physical symptoms of anxiety. Score range:0- 63, with 3 levels of severity 0-21 mild anxiety, 22-35 moderate anxiety and 36-63 severe anxiety.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
34.92
(8.6)
34.29
(10.97)
30.63
(9.53)
8 weeks
24.04
(8.84)
16.50
(8.99)
31.71
(10.26)
6 months
24.33
(9.51)
17.75
(8.72)
31.71
(10.26)
4. Secondary Outcome
Title Change From Baseline Score in the Beck Depression Inventory at 8 Weeks and 6 Months.
Description Beck Depression Inventory-II (BDI-II), Spanish adaptation (38, 39). This 21-item self-reported instrument evaluates symptoms of depression. Score range:0- 63, with 3 levels of severity, 10-18 mild depression, 19-29 moderate depression and >30 severe depression.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
18.00
(5.26)
19.46
(5.11)
19.75
(4.77)
8 weeks
11.92
(6.02)
10.71
(5.56)
19.58
(6.71)
6 months
11.63
(5.33)
10.21
(4.79)
19.58
(6.71)
5. Secondary Outcome
Title Change From Baseline Score in the Sheehan Disability Inventory (Work Subscale) at 8 Weeks and 6 Months.
Description This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
6.33
(2.53)
5.88
(2.61)
5.67
(3.29)
8 weeks
4.42
(2.55)
2.96
(2.42)
5.79
(3.09)
6 months
4.21
(2.12)
3.08
(2.33)
5.79
(3.09)
6. Secondary Outcome
Title Change From Baseline Score in the Sheehan Disability Inventory (Social Life Subscale) at 8 Weeks and 6 Months.
Description This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
6.25
(2.36)
6.83
(2.27)
5.46
(3.0)
8 weeks
4.54
(2.37)
3.75
(2.48)
5.46
(3.06)
6 months
4.33
(2.37)
3.21
(2.16)
5.46
(3.06)
7. Secondary Outcome
Title Change From Baseline Score in the Sheehan Disability Inventory (Family Subscale) at 8 Weeks and 6 Months.
Description This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
4.96
(2.75)
4.88
(2.55)
4.58
(2.99)
8 weeks
3.58
(2.33)
2.88
(2.47)
5.21
(3.12)
6 months
3.46
(2.51)
2.54
(2.57)
5.21
(3.12)
8. Secondary Outcome
Title Change From Baseline Score in the Sheehan Disability Inventory (Stress Subscale) at 8 Weeks and 6 Months.
Description This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
7.42
(1.61)
7.38
(2.37)
7.17
(2.29)
8 weeks
5.04
(2.07)
4.63
(2.88)
6.96
(2.86)
6 months
4.92
(2.10)
3.79
(2.50)
6.96
(2.86)
9. Secondary Outcome
Title Change From Baseline Score in the Sheehan Disability Inventory (Social Support Subscale) at 8 Weeks and 6 Months.
Description This 5-item instrument assesses functional impairment at work, and in social and family life. There are 5 subscales: work, social life, family life, stress, social support. The first three subscales range from 0 to 10, with higher scores indicating greater disability. The fourth subscale (stress) range from 0 to 10, with higher scores indicating greater stress perceived. The fifth subscale (Social Support Subscale) ranges from 0 to 100, with higher scores indicating greater social support perceived.There is not a total score.
Time Frame Baseline, 8 weeks, 6 months.

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
Measure Participants 24 24 24
Base line
58.75
(31.80)
60.00
(30.78)
49.58
(35.19)
8 weeks
62.92
(28.51)
72.50
(24.53)
62.92
(27.73)
6 months
68.33
(20.57)
70.00
(22.26)
62.92
(27.73)

Adverse Events

Time Frame 8 months
Adverse Event Reporting Description A weekly questionnaire regarding anxiety symptoms was administered.
Arm/Group Title Non-scheduled Support Scheduled Support Waiting List
Arm/Group Description Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone when they required it. Non-scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone when they required it. Participants received an Web-based cognitive behavioral treatment for Panic Disorder with the support of a therapist via phone weekly. Scheduled support: Participants followed the online self-help program based on cognitive behavioral therapy for 8 weeks. They had the support of a therapist via phone weekly. Participants in a waiting list.
All Cause Mortality
Non-scheduled Support Scheduled Support Waiting List
Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total / (NaN) / (NaN) / (NaN)
Serious Adverse Events
Non-scheduled Support Scheduled Support Waiting List
Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/24 (0%) 0/24 (0%) 0/24 (0%)
Other (Not Including Serious) Adverse Events
Non-scheduled Support Scheduled Support Waiting List
Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/24 (0%) 0/24 (0%) 0/24 (0%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Dr. Pablo Oromendia
Organization Universitat Autonoma de Barcelona
Phone +34 665175467
Email p.oromendia@gmail.com
Responsible Party:
Pablo Oromendia, PhD Candidate, Universitat Autonoma de Barcelona
ClinicalTrials.gov Identifier:
NCT02402322
Other Study ID Numbers:
  • PTCCAP
First Posted:
Mar 30, 2015
Last Update Posted:
Dec 7, 2015
Last Verified:
Oct 1, 2015