Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:17 AM
Ignite Modification Date:
2025-12-25 @ 4:17 AM
NCT ID:
NCT06487520
Eligibility Criteria:
Inclusion Criteria:
* Being in accordance with time and place
* Being aged between 18 and 35 years
* Being able to evaluate the visual analog scale correctly
* Participating voluntarily in the research.
* Being willing to donate blood
* Donating blood for the first time
* Have a body mass index within normal limits (18.5-24.9 kg/m2)
* Have no vision or hearing problems
* Have no disease that may affect pain perception
* Have no vertigo, heart or lung disease
* Have no signs of infection, dermatitis, phlebitis, scar tissue or incision in the area where invasive intervention will be performed
* Have no psychiatric disease
* Being able to accurately assess the state and trait anxiety inventory with the VAS
* Have an average pressure pain threshold value of 8-16 Lb obtained from three measurements taken at 5-second intervals from the elbow region of the left upper extremity where no intervention was performed
* Have no vertigo, heart or lung disease
* Have no signs of infection, dermatitis, phlebitis, scar tissue or incision in the area where invasive intervention will be performed
* Have no psychiatric disease
* Being able to accurately assess the state and trait anxiety inventory with the VAS
* Have an average pressure pain threshold value of 8-16 pounds (Lb) obtained from three measurements taken at 5-second intervals from the elbow region of the left upper extremity where no intervention was performed
Exclusion Criteria:
* Not participating voluntarily in the research
* Not fitting the inclusion criteria of the research
* Having a vision or hearing problem
* Failure of phlebotomy at the first attempt
* Development of syncope after phlebotomy
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT06487520
Study Brief:
Protocol Section:
NCT06487520