Effect of Different Subcutaneous Injection Methods on Pain and Satisfaction
NCT ID: NCT06829407
Last Updated: 2025-02-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
112 participants
INTERVENTIONAL
2024-08-20
2024-09-23
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Vibration Anesthesia on Pain, Ecchymosis and Comfort Level in Subcutaneous Heparin Injection
NCT06662240
Effect of Shotblocker and Palm Stimulator
NCT06381804
The Effect of Vibration on Pain During Subcutaneous Heparin Injection
NCT06469112
Effects of Vibration, Heel Warming and Shotblocker on Pain Levels During Heel Blood Collection
NCT06646848
The Effect of Vibration Application on Pain and Satisfaction Associated With Subcutaneous Anticoagulation Injection
NCT05686148
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
injection time
The application will be done by injecting for 30 seconds and then waiting for 10 seconds and ending the process.
injection time
give an injection
palm stimulator
By ensuring that the patient grasps the "palm stimulator" equipment in the palm during the injection and squeezes it in the palm throughout the injection. Tactile warning will be given. However, the injection process will last 10 seconds and the process will be terminated after waiting 10 seconds.
palm stimulator
give an injection
injection time and palm stimulator
Injection will be done for 30 seconds and then waited for 10 seconds and the process will be terminated, and the application will be done using equipment.
injection time and palm stimulator
give an injection
control group
The injection process will last 10 seconds and the process will be terminated after waiting 10 seconds.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
injection time
give an injection
palm stimulator
give an injection
injection time and palm stimulator
give an injection
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The one who is literate,
* No physical, mental disabilities or communication difficulties,
* Low Molecular Weight Heparin in the treatment plan,
* No history of allergy,
* Agreeing to participate in the research,
* There is no scar tissue, incision or infection in the area to be injected,
* Patients who will receive a 1-day injection and whose pain score is between 1-10 according to VAS will be admitted.
Exclusion Criteria
* Using subcutaneous insulin therapy,
* There is an amputation in the right/left arm area where the study will be performed,
* There is scar tissue, incision or signs of infection in the area to be injected,
* Patients who received injections for 1 day and whose pain score is 0 (zero) according to VAS will not be admitted.
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Trakya University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ali Umit Yilmaz
Nurse
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Trakya Üniversitesi
Edirne, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TUTF-GOBAEK 202313|8
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.