- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01753284
First Episode Psychosis and Pathway to Care in Nordland
May 10, 2019 updated by: Nordlandssykehuset HF
Patients and Carers Experiences With First Episode Psychosis and Pathway to Care in Nordland: A Qualitative Study
First episode psychosis patients often experiences treatment delay.
This reduces their prospects for recovery and makes unnecessary burdens for them and their carers.
A better understanding of help seeking intentions is required, and has not been explored in a county like Nordland, Norway, with long distances and challenging access to health services.
The purpose of this study is to explore the process of help seeking, including how patients and their careers discover and understand the psychotic symptoms.
Research exploring the impact on families mainly focuses on parents' experiences, and there are less studies focusing on experiences and needs of siblings.
This study will therefore explore siblings' experiences separate from their parents.
Methods will be qualitative interviews with patients, their carers and siblings.
Analysis will be influenced by Grounded theory.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
40
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years to 35 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients experiencing first and multiple episode psychosis carers siblings
Description
Inclusion Criteria:
- age 16-35,
- understand and speak Norwegian
- able to give consent
- no learning disabilities
Exclusion Criteria:
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Patient experience
Time Frame: up to 100 weeks
|
up to 100 weeks
|
Carers experiences
Time Frame: up to 100 weeks
|
up to 100 weeks
|
Siblings experiences
Time Frame: up to 100 weeks
|
up to 100 weeks
|
Pathway to care
Time Frame: up to 100 weeks
|
up to 100 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2013
Primary Completion (Actual)
October 1, 2018
Study Completion (Actual)
December 1, 2018
Study Registration Dates
First Submitted
December 17, 2012
First Submitted That Met QC Criteria
December 19, 2012
First Posted (Estimate)
December 20, 2012
Study Record Updates
Last Update Posted (Actual)
May 13, 2019
Last Update Submitted That Met QC Criteria
May 10, 2019
Last Verified
April 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2012/1650(REK)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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