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NCT03168789
Tension Tamer Randomized Control Trial
NA trial testing Tension Tamer (TT) in Pre-hypertension in 80 participants. Completed in 22 November 2019.
22 November 2019
Quick facts
| Lead sponsor | Medical University of South Carolina |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 80 |
| Start date | 1 October 2016 |
| Primary completion | 22 November 2019 |
| Estimated completion | 22 November 2019 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Tension Tamer (TT)
- Lifestyle education program (SPCTL)
Conditions studied
- Pre-hypertension — all drugs for Pre-hypertension →
Sponsor
Medical University of South Carolina
Who can join
Adults 18 to 90, any sex, with Pre-hypertension. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study is 12 months long and consists of 5 visits at baseline, months 1, 3, 6, and 12. To determine eligibility potential subjects will have resting blood pressures (BP) measured on 2 occasions. Pre-hypertensive individuals will be invited to participate in the study. After informed consent is obtained, subjects will complete baseline visit consisting of a survey, resting BP, wear activity watch for 7 days ambulatory blood pressure monitor for 24-hours, collect saliva and urine samples. Subjects will then be randomly assigned to Tension Tamer (TT) or lifestyle education program delivered via smartphone (SPCTL) groups. At the remaining 4 visits subjects will again complete a survey, resting BP, wear activity watch for 7 days ambulatory blood pressure monitor for 24-hours, collect saliva and urine samples. Throughout the 12 months TT group will meditate twice daily and SPCTL group will log physical activity.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Meditation smartphone application effects on prehypertensive adults' blood pressure: Dose-response feasibility trial.
Adams ZW, Sieverdes JC, Brunner-Jackson B, Mueller M, et al · · 2018 · cited 26× · PMID 30010353 · DOI 10.1037/hea0000584 -
Impact of 12-Month Smartphone Breathing Meditation Program upon Systolic Blood Pressure among Non-Medicated Stage 1 Hypertensive Adults.
Chandler J, Sox L, Diaz V, Kellam K, et al · · 2020 · cited 17× · PMID 32192020 · DOI 10.3390/ijerph17061955 -
The Recent Advances of Mobile Healthcare in Cardiology Practice.
Kulbayeva S, Tazhibayeva K, Seiduanova L, Smagulova I, et al · · 2022 · cited 5× · PMID 36311150 · DOI 10.5455/aim.2022.30.236-250
Verify or expand the search:
- PubMed search for NCT03168789
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Pre-hypertension
Currently open trials in the same condition.
- NCT05892328 — Watermelon Dose Response Blood Pressure Study · NA · active not recruiting
Other Medical University of South Carolina trials
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03168789 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Medical University of South Carolina
- Last refreshed: 14 January 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03168789.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing