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A preliminary investigation of the efficacy of an enhanced Cognitive Behavioural Treatment Program for Excessive Worry.

A preliminary investigation of the efficacy of an enhanced Cognitive Behavioural Treatment Program for Excessive Worry in individuals with Generalized Anxiety Disorder (GAD) using a case studies design.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000807257
Enrollment
8
Registered
2009-09-16
Start date
2009-09-20
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Generalized Anxiety Disorder (GAD) is a disabling disorder characterized by the central defining feature of pervasive, excessive and uncontrollable worry. Although the traditional Cognitive Behavioural Therapy (CBT) has been found to be effective for GAD patients, a significant proportion of these patients fail to achieve high end-state functioning. Recent research evidence have found GAD to be associated with a person's intolerance of uncertainty, unhelpful meta-cognitions, and deficits in emotional regulation. The current study thus aims to investigate the efficacy of an enhanced CBT treatment that teaches GAD patients skills in managing emotions, uncertainty and unhelpful meta-cognitions, in addition to the usual CBT skills. It is hypothesized that GAD-related symptoms in the patients will improve with the enhanced CBT treatment and the change of symptoms will be related to change in scores (baseline to post-treatment) in one or more of the aforesaid factors (i.e. emotion regulation, meta-cognitions and/or intolerance of uncertainty).

Interventions

Cognitive Behavioural Therapy a) the duration & frequency of therapy sessions: 12 x 1-hour sessions on a weekly basis. b) the overall duration of the therapy program: 12 weeks. c) the mode of administration: one-on-one sessions with a psychologist. d) the topics covered: managing emotions, uncertainty and unhelpful meta-cognitions.

Sponsors

Hock Lai CHOO, Christopher
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must be 18 years old or older, and must meet the DSM-VI criteria for a primary diagnosis of GAD as assessed on the ADIS-IV.

Exclusion criteria

Patients who are psychotic, suicidal or have significant substance abuse problems.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026