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Trial · NCT07880496

The Effect of ShotBlocker on Symptoms of Pain, Anxiety, and Cortisol Hormone Levels

NCT07880496, Not applicable, Not yet recruiting, Ataturk University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. The Effect of ShotBlocker on Symptoms of Pain, Anxiety, and Cortisol Hormone Levels. Trials, record NCT07880496. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07880496

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
The Effect of ShotBlocker on Symptoms of Pain, Anxiety, and Cortisol Hormone Levels
NCT number
NCT07880496
Status
Not yet recruiting
Phases
Not applicable
Enrollment
68 participants, estimated
Lead sponsor
Ataturk University
Conditions
Pain, Anxiety
Interventions
Intervention Group, Control
First posted
2026-10-19
Last updated
2026-11-03

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPersonal Information FormAt baseline, before the intervention
This form, created by the researcher, contains a total of 8 questions covering the patients' age, gender, education level, marital status, height/weight, body mass index, and questions about their illness.
PrimaryVisual Analog Scale10 minutes before and 10 minutes after the lumbar puncture procedure
This scale ranges from 0, indicating "No pain," to 10, indicating "Unbearable pain." The patient is asked to rate the intensity of pain on a scale from 0 to 10. The selected value represents the patient's pain score.
PrimaryState Anxiety Scale10 minutes before and 10 minutes after the lumbar puncture procedure
The State-Trait Anxiety Inventory (STAI) assesses anxiety in individuals aged 14 years and older. The 20-item State Anxiety Inventory used in this study is a 4-point Likert scale: "not at all" (1), "somewhat" (2), "moderately so" (3), and "very much so" (4). Items 1, 2, 5, 8, 10, 11, 15, 16, 19, and 20 are reverse-scored (1=4, 2=3, 3=2, 4=1). Scores are summed according to the scoring procedure, with a constant value of 50 added to obtain the final anxiety score. Total scores range from 20 to 80, with higher scores indicating greater anxiety.
PrimarySalivary Cortisol Level10 minutes before and 30 minutes after the lumbar puncture procedureSalivary cortisol levels will be measured using commercially available kits with the ELISA method.

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT07880496

GET https://conductscience.org/api/trials/v1/NCT07880496/registered