Effects of an Anxiety-Reduction Program in Adults Undergoing Awake Hand Surgery
NCT07918482, Not applicable, Completed, Muhammet Okkan
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effects of an Anxiety-Reduction Program in Adults Undergoing Awake Hand Surgery | ClinicalTrials.gov |
| NCT number | NCT07918482 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 120 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Muhammet Okkan | ClinicalTrials.gov |
| Conditions | Anxiety | ClinicalTrials.gov |
| Interventions | Structured Multicomponent Anxiety-Reduction Protocol | ClinicalTrials.gov |
| First posted | 2026-11-05 | ClinicalTrials.gov |
| Last updated | 2026-11-05 | ClinicalTrials.gov |
Registered outcomes 5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Postoperative State Anxiety Score Measured by the State-Trait Anxiety Inventory (STAI-I) | 10-30 minutes after completion of surgery, before patient discharge. | Postoperative state anxiety was assessed using the validated Turkish version of the State form of the State-Trait Anxiety Inventory (STAI-I). The questionnaire consists of 20 items, with total scores ranging from 20 to 80. Higher scores indicate greater state anxiety. The primary outcome was the total STAI-I score measured approximately 10-30 minutes after surgery, before patient discharge. Postoperative STAI-I scores were compared between the intervention and control groups using analysis of covariance (ANCOVA), adjusted for preoperative STAI-I scores. | ClinicalTrials.gov |
| Secondary | Pain During Local Anesthetic Injection Assessed Using a Visual Analogue Scale (VAS) | Immediately after local anesthetic injection, during the surgical visit. | Injection-related pain was assessed immediately after local anesthetic administration using a 0-10 visual analogue scale (VAS). A score of 0 indicates no pain, while a score of 10 indicates the worst imaginable pain. Higher scores represent greater pain intensity during local anesthetic injection. | ClinicalTrials.gov |
| Secondary | Postoperative Patient Satisfaction Score Assessed Using a 5-Point Rating Scale | Day 1 (postoperative, 10-30 minutes after surgery) | Patient satisfaction with the WALANT surgical experience was assessed after completion of surgery using a 5-point rating scale: 1 = not at all satisfied, 2 = slightly satisfied, 3 = moderately satisfied, 4 = very satisfied, and 5 = completely satisfied. Higher scores indicate greater patient satisfaction. | ClinicalTrials.gov |
| Other | Number of Participants Willing to Undergo WALANT Again | Day 1 (postoperative, 10-30 minutes after surgery) | Participants were asked after surgery whether they would choose the WALANT technique again if another surgical procedure were needed. The outcome was the number of participants who answered "Yes" in each study group, indicating willingness to undergo WALANT again. | ClinicalTrials.gov |
| Other | Number of Participants Willing to Recommend WALANT to Others | Day 1 (postoperative, 10-30 minutes after surgery) | Participants were asked after surgery whether they would recommend the Wide-Awake Local Anesthesia No Tourniquet (WALANT) technique to others. Responses were recorded as Yes or No. The outcome was the number of participants who answered "Yes" in each study group, indicating willingness to recommend WALANT to others. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)