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Completed

NCT Number: NCT06829407

Effect of Different Subcutaneous Injection Methods on Pain and Satisfaction

This study; In patients treated with subcutaneous heparin A randomized controlled trial was planned to determine the effect of the injection time and the device called "Palm Stimulator" to reduce the pain felt during injection.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Trakya Üniversitesi

Edirne, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Above 18 years old
  • 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

  • Who gave up participating in the research while continuing the research,
  • 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.

Treatment and study plan

injection time

Other

give an injection

palm stimulator

Other

give an injection

injection time and palm stimulator

Other

give an injection

Primary outcomes

  1. Scale Patient Identification Form

    Time frame: during injection procedure

    Patient Identification Form

    It was prepared by researchers by examining the literature on the subject. This form includes 5 questions that include some sociodemographic characteristics of the individual (age, gender, marital status, education status, employment status, etc.) and 8 questions that include characteristics related to health, illness and treatment (presence of chronic disease, body mass index, etc.).

  2. Visual Scale for pain

    Time frame: during injection procedure

    Visual comparison scale for pain The scale consists of a single item, the scale is formed by a 10 cm long line on the horizontal plane. The leftmost side of the line (starting point) is scored as 0 (zero) and the rightmost side (ending point) is scored as 10 (ten) points for the highest possible pain. In order for the patient to score the pain, he/she is asked to mark a point on the line during the injection process. After marking, the distance from the starting point to the marked place is measured and the score is formed. The scale has been proven to be reliable in terms of Turkish as a result of the study conducted by Yaray et al.

  3. Visual Comparison Scale for Satisfaction

    Time frame: during injection procedure

    Visual Comparison Scale for Satisfaction In this scale, scores between 0 and 10 were used to determine satisfaction levels. A score of 0 represented the least satisfaction level, while a score of 10 represented the highest satisfaction level. The Visual Analog Scale was used so that patients could express both their pain and satisfaction levels.

Sponsors and collaborators

Lead sponsor

Trakya University

Other

Registry information

Official study title

Evaluation of the Effects of Different Methods Used in Subcutaneous Heparin Injections on Pain and Satisfaction

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Feb 17, 2025
Registry last updated
Feb 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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