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Comparison of Fasting Blood Glucose Measurements From Fingertip and Intravenous on Patient Satisfaction in Patients With Diabetes Mellitus

Primary Purpose

Diabetes Mellitus

Status
Recruiting
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Patients whose blood glucose is measured intravenously and from the fingertip
Sponsored by
Istanbul University - Cerrahpasa (IUC)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Diabetes Mellitus focused on measuring Diabetes mellitus, Fear of finger piercing, patient satisfaction, blood glucose measurement

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: 18 years and older No advanced hearing and vision problems Able to speak and understand Turkish Easy to communicate literate Agreeing to participate in the research voluntarily Patients who are hospitalized Regular finger blood sugar monitoring, Patients with an intravenous vascular access date within the first 24 hours Patients who had been diagnosed with Type 2 Diabetes Mellitus for at least one year were. Exclusion Criteria: Those who are treated with sedative drugs Patients using antipsychotic medication Patients with continuous drug infusion through the intravenous line Patients whose intravenous vascular access date has passed 24 hours Patients in unconscious, confused, apathetic state

Sites / Locations

  • Istanbul University-Cerrahpaşa (IUC)Recruiting
  • Istanbul University-Cerrahpaşa (IUC)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

experimental group

control group

Arm Description

Patients whose blood glucose is measured intravenously and from the fingertip

Patients with fingertip blood glucose measurement

Outcomes

Primary Outcome Measures

Blood Glucose Measurement Patient Satisfaction Form
Does intravenous blood glucose measurement have a positive effect on patient satisfaction compared to fingertip blood glucose measurement?

Secondary Outcome Measures

Full Information

First Posted
July 20, 2023
Last Updated
July 28, 2023
Sponsor
Istanbul University - Cerrahpasa (IUC)
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1. Study Identification

Unique Protocol Identification Number
NCT05976191
Brief Title
Comparison of Fasting Blood Glucose Measurements From Fingertip and Intravenous on Patient Satisfaction in Patients With Diabetes Mellitus
Official Title
Istanbul University Cerrahpaşa-IUC
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2023 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Istanbul University - Cerrahpasa (IUC)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study was designed as a randomized controlled experimental study in order to compare the fasting blood glucose values measured by puncturing the fingertips and using the intravenous route of patients diagnosed with diabetes mellitus, and to determine the effect on patient satisfaction. The blood glucose measurement via the intravenous catheter has an effect on increasing the comfort of the patient compared to the fingertip measurement. It is thought that information can be provided to increase patient satisfaction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus
Keywords
Diabetes mellitus, Fear of finger piercing, patient satisfaction, blood glucose measurement

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Crossover Assignment This research was designed in a pretest posttest randomized controlled experimental type
Masking
Participant
Masking Description
Single (Participant) Identity information of the patients was concealed and verbal and written consents were obtained.
Allocation
Randomized
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
experimental group
Arm Type
Experimental
Arm Description
Patients whose blood glucose is measured intravenously and from the fingertip
Arm Title
control group
Arm Type
No Intervention
Arm Description
Patients with fingertip blood glucose measurement
Intervention Type
Behavioral
Intervention Name(s)
Patients whose blood glucose is measured intravenously and from the fingertip
Intervention Description
A satisfaction survey will be conducted after these patients have previously examined their blood glucose via intravenous route, then fingertip blood glucose will be measured and a satisfaction survey will be applied.
Primary Outcome Measure Information:
Title
Blood Glucose Measurement Patient Satisfaction Form
Description
Does intravenous blood glucose measurement have a positive effect on patient satisfaction compared to fingertip blood glucose measurement?
Time Frame
four months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years and older No advanced hearing and vision problems Able to speak and understand Turkish Easy to communicate literate Agreeing to participate in the research voluntarily Patients who are hospitalized Regular finger blood sugar monitoring, Patients with an intravenous vascular access date within the first 24 hours Patients who had been diagnosed with Type 2 Diabetes Mellitus for at least one year were. Exclusion Criteria: Those who are treated with sedative drugs Patients using antipsychotic medication Patients with continuous drug infusion through the intravenous line Patients whose intravenous vascular access date has passed 24 hours Patients in unconscious, confused, apathetic state
Facility Information:
Facility Name
Istanbul University-Cerrahpaşa (IUC)
City
Istanbul
State/Province
Şişli
ZIP/Postal Code
34381
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
AYSEGUL OZBAKAN
Phone
00905423047687
Email
aysegulozbakan@icloud.com
First Name & Middle Initial & Last Name & Degree
ARZU ERKOC
Phone
00905552735500
Email
arzu.erkochut@iuc.edu.tr
Facility Name
Istanbul University-Cerrahpaşa (IUC)
City
Istanbul
State/Province
Şişli
ZIP/Postal Code
34381
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
AYSEGUL OZBAKAN
Phone
05423047687
Email
aysegulozbakan@icloud.com
First Name & Middle Initial & Last Name & Degree
ARZU ERKOÇ
Phone
05552735500
Email
arzu.erkochut@iuc.edu.tr

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparison of Fasting Blood Glucose Measurements From Fingertip and Intravenous on Patient Satisfaction in Patients With Diabetes Mellitus

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