Shot blocker reducing pain from subdermal single-rod contraceptive implantation contraception, pain
Conditions
Interventions
Participants will receive the single-rod contraceptive implantation using the ShotBlocker device. The device will be pressed firmly against the skin at the insertion site to elicit mechanical stimulat
Experimental Device,No Intervention No treatment
shotblocker,routine care
Sponsors
Faculty of Medicine, Thammasat University
Eligibility
Sex/Gender
Female
Age
13 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1. Clients receiving insertion of a single-rod contraceptive implant at the Family Planning Unit of Thammasat University Hospital 2. Aged 13 to 50 years
Exclusion criteria
Exclusion criteria: 1. Request removal of a previous contraceptive implant and insertion of a new implant during the same visit. 2. Dermatological issues, such as skin infections or lesions at the intended implant site. 3. Sensory impairment, such as peripheral neuropathy. 4. Psychiatric disorders 5. Do not provide consent to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain score anticipated pain before implant insertion, pain during local anesthesia injection, pain during implant insertion, and 15 minutes after implant insertion visual analog scale | — |
Secondary
| Measure | Time frame |
|---|---|
| anxiety level before implant insertion, during implant insertion, and 15 minutes after implant insertion. visual analog scale | — |
Countries
Thailand
Contacts
Public ContactPhanthira Limphanudom
Faculty of Medicine, Thammasat University
Outcome results
None listed