Trial · NCT07889739
Sensation Seeking and TMS Response in TRD
NCT07889739, Recruiting, Technical University of Munich
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Sensation Seeking and TMS Response in TRD. Trials, record NCT07889739. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889739
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Sensation Seeking and TMS Response in TRD
- NCT number
- NCT07889739
- Status
- Recruiting
- Enrollment
- 100 participants, estimated
- Lead sponsor
- Technical University of Munich
- Conditions
- MDD, Severe Depression, Major Depressive Episode
- Interventions
- Transcranial Magnetic Stimulation (TMS)
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Correlation Between Change in Montgomery-Åsberg Depression Rating Scale (MADRS) Scores and Baseline Sensation Seeking Scale (SSS) Total Score | Baseline (within 7 days before first TMS session) to end of acute TMS course (approximately 4-6 weeks) | The primary analysis will test the correlation between change in depressive symptom severity (ΔMADRS = baseline MADRS - end-of-treatment MADRS) and the baseline Sensation Seeking Scale total score. Pearson's or Spearman's correlation coefficient (r/ρ) will be calculated, with 95% confidence intervals. |
| Secondary | Association Between Change in MADRS and SSS Total Score (Adjusted Model) | Baseline to end of acute TMS (4-6 weeks) | Multivariable linear regression of ΔMADRS on baseline SSS total, adjusting for age, sex, baseline MADRS, treatment parameters, and TRD burden. |
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/NCT07889739
GET https://conductscience.org/api/trials/v1/NCT07889739/registered