The Effect of Transcutaneous Electrical Nerve Stimulation (TENS) on Pain, Mobilization, and Insomnia Severity After Cesarean Section: A Randomized Controlled Trial
NCT07933263, Not applicable, Active not recruiting, Inonu University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | The Effect of Transcutaneous Electrical Nerve Stimulation (TENS) on Pain, Mobilization, and Insomnia Severity After Cesarean Section: A Randomized Controlled Trial | ClinicalTrials.gov |
| NCT number | NCT07933263 | ClinicalTrials.gov |
| Status | Active not recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 72 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Inonu University | ClinicalTrials.gov |
| Conditions | Postoperative Pain After Cesarean Section, Early Postpartum Mobilization, Postpartum Sleep | ClinicalTrials.gov |
| Interventions | Tens | ClinicalTrials.gov |
| First posted | 2026-11-12 | ClinicalTrials.gov |
| Last updated | 2026-11-12 | ClinicalTrials.gov |
Registered outcomes 4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Postoperative Pain Severity | Before TENS application and before discharge (0-48 hours) | Pain intensity will be assessed using the Visual Analog Scale (VAS). The objective is to determine the effectiveness of TENS in reducing postoperative pain following a cesarean section. | ClinicalTrials.gov |
| Secondary | Level of Mobilization (Patient Mobility Scale - PMS) | Before TENS application and before discharge (0-48 hours) | The levels of pain and exertion experienced by participants while turning in bed, sitting at the edge of the bed, standing up, and walking around the room will be assessed using a five-point Likert-type scale. | ClinicalTrials.gov |
| Secondary | Level of Independence (Observer Mobility Scale - OMS) | Before TENS application and before discharge (0-48 hours) | The independence levels of the participants will be scored on a scale from 1 (completely independent) to 5 (completely dependent). | ClinicalTrials.gov |
| Secondary | Insomnia Severity (Insomnia Severity Index - ISI) | Before TENS application and before discharge (0-48 hours) | The severity of insomnia will be assessed using the seven-item Insomnia Severity Index (ISI). The scale measures sleep onset, sleep maintenance, early awakening, sleep satisfaction, impairment in daily functioning, and stress levels. | 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 |
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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)