Ignite Creation Date:
2024-05-06 @ 3:02 PM
Last Modification Date:
2024-10-26 @ 1:41 PM
Study NCT ID:
NCT04502836
Status:
TERMINATED
Last Update Posted:
2024-04-12
First Post:
2020-07-26
Brief Title:
Evaluation of the Correlation Between Psychological Intervention Including Providing Knowledge and Tools for Problems Solving and the Anxiety Level of Female Patients Arriving to ACTH LRH Test - Pilot Study
Sponsor:
Rabin Medical Center
Organization:
Rabin Medical Center
Study Overview
Official Title:
Evaluation of the Correlation Between Psychological Intervention Including Providing Knowledge and Tools for Problems Solving and the Anxiety Level of Female Patients Arriving to ACTH LRH Test - Pilot Study
Status:
TERMINATED
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
internal reasons
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Over 20 of the population is reporting on white coat syndrome manifested as anxiety symptoms and elevated BP during interaction with medical staff It is estimated that throughout the life span of children approximately 15-20 will suffer from some form of a trauma relating to an interaction with health provider The proposed study aims is to evaluate the correlation between a single preliminary psychological intervention including providing knowledge and tools for problems solving and the anxiety level in female patients arriving to Adrenocorticotropic Hormone ACTH and Lutenising Releasing Hormone LRH test in comparison to the anxiety in patients arriving to the same test without psychological intervention 20 female patients arriving to ACTH LRH test for puberty stage assessment performed as part of routine medical care will be recruited to the study and will be randomized to one of 2 groups Participants in the intervention group 10 patients will be required to arrive with their parents an hour prior to the test and will receive a preliminary psychological intervention The control group will arrive to the ACTH LRH test on the scheduled time and will not receive psychological intervention
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None