Trial · NCT07892365
The Effect of Chewing Gum on Pain and State Anxiety During Intravenous Blood Sampling
NCT07892365, Not applicable, Completed, Dicle University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of Chewing Gum on Pain and State Anxiety During Intravenous Blood Sampling. Trials, record NCT07892365. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07892365
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of Chewing Gum on Pain and State Anxiety During Intravenous Blood Sampling
- NCT number
- NCT07892365
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 170 participants, actual
- Lead sponsor
- Dicle University
- Conditions
- Intravenous Blood Sampling, Pain and Anxiety
- Interventions
- Chewing gum was done during the intravenous blood draw procedure
- First posted
- 2026-10-23
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | pain level-Visual Analog Scale (VAS) | Before and immediately after the intravenous blood sampling procedure. | Pain level was assessed using the Visual Analog Scale (VAS) before and after the intravenous blood sampling procedure in both the experimental and control groups. The Visual Analog Scale, used to measure pain intensity, is a one-dimensional scale measuring 0-10 cm (0-100 mm) in length. 0 cm means no pain, 10 cm means unbearable pain. As the score increases, the pain intensity increases. On the scale, 0-4 mm is defined as 'no pain', 4-6 mm is defined as 'slight pain', 7-9 mm is defined as 'moderate pain', 10 mm is defined as 'severe pain'. |
| Primary | state anxiety level- state anxiety inventory(STAI-I) | Before and immediately after the intravenous blood sampling procedure. | State anxiety was assessed using the State Anxiety Inventory (STAI-I) before and after the intravenous blood sampling procedure in both the experimental and control groups. The State Anxiety Inventory (STAI-I) uses a four-point Likert scale (1: Not at all, 2: Somewhat, 3: Very much, 4: Completely). Directly scored items reflect negative emotions, whereas reverse-scored items reflect positive emotions. The State Anxiety Inventory (STAI-I) includes 10 reverse-scored items (items 1, 2, 5, 8, 10, 11, 15, 16, 19, and 20) (140, 148). The total score ranges from 20 to 80, with scores of 20-39 indicating mild anxiety, 40-59 indicating moderate anxiety, and 60-79 indicating high anxiety. Scores of 60 or above are considered indicative of a need for professional support. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07892365
GET https://conductscience.org/api/trials/v1/NCT07892365/registered