- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05679804
Turkish Validity and Reliability Study of The Bipolar Recovery Questionnaire
December 24, 2022 updated by: Zehra GÜNAY YAĞCI, Bilecik Seyh Edebali Universitesi
In addition to objective criteria (no episode period for 6 months) for defining and monitoring recovery, evaluation of subjective criteria is also very important.
Various Turkish scales related to recovery in progressive diseases have been developed or validity-reliability studies have been conducted.
However, as far as we know, there is no scale that evaluates subjective improvement for a disorder such as bipolar disorder that progresses in episodes and has a heterogeneous appearance of loss of functionality.
In this study, we aimed to conduct a validity and reliability study of the recovery questionnaire for BDD.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Bilecik, Turkey, 11000
- Bilecik Seyh Edebali University Faculty of Medicine
-
-
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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Bipolar Affective Disorder
Description
Inclusion Criteria:
- Being between 18-65 ages
- Be diagnosed with bipolar affective disorder
- Be at least primary school graduate
Exclusion Criteria:
- having a physical disability (blindness, etc.) that might prevent filling in the scales,
- having an additional neurological disease that prevented filling out the scale items.
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
validity and reability of scale
Time Frame: 5 months
|
turkish validity and reability of Bipolar Recovery Questionnare
|
5 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
December 13, 2022
Primary Completion (Anticipated)
April 13, 2023
Study Completion (Anticipated)
May 13, 2023
Study Registration Dates
First Submitted
December 24, 2022
First Submitted That Met QC Criteria
December 24, 2022
First Posted (Estimate)
January 11, 2023
Study Record Updates
Last Update Posted (Estimate)
January 11, 2023
Last Update Submitted That Met QC Criteria
December 24, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BilecikSeyhEU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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