The Effect of Cold Compression on the surgical site post subdermal contraceptive implantation procedure to reduce Pain and bruise among adolescents and young women in Family Planning Clinic.

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

TCTR

Registry ID

TCTR20250222007

Enrollment

Registered

2025-02-22

Start date

2025-03-18

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bruising around the surgical site post-subdermal contraceptive implantation procedures Pain around the surgical site post-subdermal contraceptive implantation procedures Bruising Pain Cold compression Contraceptive implantation

Interventions

The protocol for applying cold compression to the surgical site of the contraceptive implant procedure, such as: Pre-procedure: applying a cold compression for 5 minutes before starting the implant pr

the pre-procedure stage, the during-procedure stage, and the post-procedure stage.

Experimental Behavioral,Active Comparator Behavioral

Cold compression care and standard nursing care for contraceptive implant procedure,Standard nursing care for contraceptive implant procedure

Eligibility

Sex/Gender

Female

Age

18 Years to 24 Years

Inclusion criteria

Inclusion criteria: Participants must be adolescents or young women 18-24 years of age. Participants are not pregnant. Participants who recieve the standard screening to use contraceptive implantation. Participants are presenting to Family Planning first time. Participants must not have a coagulation disorder and/or must not use anticoagulant drugs during treatment. Participants must not have underlying cold allergies. Participants must not have any bruising and pain (VAS = 0) around the surgical site areas. Participants must be able to understand and communicate in Thai language. Participants must have a smartphone or a device for follow-up phone calls and Line application. Participants must have a refrigerator or device to keep the cool temperature.

Exclusion criteria

Exclusion criteria: Participants take some medicines to relief pain during to time collection. Participants have medical supplies allergies. Participants can not follow up on the process of study to end time.

Design outcomes

Primary

Measure	Time frame
Bruise size 4 L-Shape standard scale Ruler	—

Secondary

Measure	Time frame
Pain scores 5 The Visual Analog Scale measurement tool	—

Countries

Thailand

Contacts

Public ContactRattiya Chuchot

Srisavarindhira Thai Red Cross Institute of Nursing

Rattiya.c@stin.ac.th0897627803

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026