None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: women in the reproductive age group attending routine clinical care services
Exclusion criteria
Exclusion criteria: 1 Women with significant comorbidities that can affect the study outcomes like abnormal pain perception, bleeding or clotting disorders, and reduced peripheral perfusion. 2 Women suffering from physical disability or/ and poor motor skills of upper limb 3 Women presenting with oedema or open wounds, abnormal skin integrity on the upper arm, subcutaneous implants in the upper arm, and known stainless steel allergies. 4 Women who cannot give consent due to any cognition or mental disabilities.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric Pain Rating scale, statistical significance of difference between mean pain scores (TAP Micro Select vs venous blood collection) will be tested using paid T test for difference between two means.Timepoint: Individuals will undergo blood sampling once at the time of recruitment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Volume of blood collected by TAP MicroSelect device.Timepoint: Individuals will undergo blood sampling once at the time of recruitment.;Net Promoter Score for TAP MicroSelect DeviceTimepoint: Individuals will undergo blood sampling once at the time of recruitment.;Ease of doing the procedure using TAP MicroSelect DeviceTimepoint: Individuals will undergo blood sampling once at the time of recruitment.;Time duration of blood collection using TAP MicroSelect deviceTimepoint: Individuals will undergo blood sampling once at the time of recruitment.;Diagnostic Accuracy of nutritional and infectious disease tests on blood collected through TAP MicroSelect as compared to blood collected using venous blood collection.Timepoint: Individuals will undergo blood sampling once at the time of recruitment. | — |
Countries
India
Contacts
St Johns Research Institute