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Clinical Trials/ACTRN12619001535167
ACTRN12619001535167
Completed
未知

Developing and evaluating an internet-delivered treatment specifically targeting repetitive negative thinking in people with elevated repetitive negative thinking- A Pilot Study

niversity of New South Wales0 sites26 target enrollmentNovember 6, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Depression
Sponsor
niversity of New South Wales
Enrollment
26
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 6, 2019
End Date
July 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • \* Score above 27 on Repetitive Negative Thinking Questionnaire.
  • \* Australian resident status
  • \* At least 18 years of age
  • \* Access to a computer, printer, and the internet
  • \* If taking medication, must have been taking the same dose for at least 2 months and not intend to change that dose during the course of the program.
  • \* Prepared to provide name, phone number, and address, and to provide the name and phone number of a local general practitioner.
  • \* Willing to provide informed consent.

Exclusion Criteria

  • \- Currently experiencing severe depression symptoms (score of 23 or above on the PHQ\-9\).
  • \- Regularly using illicit drugs or regularly consuming more than three standard drinks per day
  • \- Current regular use of benzodiazepines
  • \- Current use of atypical anti\-psychotics
  • \- Currently experiencing a psychotic mental illness or bipolar disorder
  • \- Completed an online program for depression and/or anxiety in the past year
  • \- Currently suicidal and/or severe symptoms of suicidal ideation (defined as responding 3 to the PHQ\-9 question 9 item that assesses the frequency of suicidal ideation over the past fortnight).
  • \-Those scoring 1 or 2 on the Patient Health Questionnaire\-9 Item (PHQ\-9\) item 9 will require risk assessment with the responsible clinician before being admitted into the study.

Outcomes

Primary Outcomes

Not specified

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