Last reviewed · How we verify
NCT04136041
Study Protocol for a Smartphone Application-based Intervention for Subthreshold Depression
NA trial testing Smartphone Application in Subthreshold Depression in 32 participants. Completed in 5 March 2020.
5 March 2020
Quick facts
| Lead sponsor | Kibi International University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 32 |
| Start date | 29 October 2019 |
| Primary completion | 5 March 2020 |
| Estimated completion | 5 March 2020 |
| Sites | 1 location across Japan |
Drugs / interventions tested
- Smartphone Application
Conditions studied
- Subthreshold Depression — all drugs for Subthreshold Depression →
Sponsor
Kibi International University
Who can join
18 and older, any sex, with Subthreshold Depression. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The investigators plan to conduct a randomized controlled trial to examine whether a Smartphone-based Intervention improves subthreshold depression symptoms compared to no intervention. The purpose of this pilot randomized controlled trial is to investigate the feasibility of the final randomized controlled trial.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Study protocol for a pilot randomized controlled trial on a smartphone application-based intervention for subthreshold depression: Study protocol clinical trial (SPIRIT Compliant).
Kato Y, Kageyama K, Mesaki T, Uchida H, et al · · 2020 · cited 4× · PMID 31977910 · DOI 10.1097/md.0000000000018934
Verify or expand the search:
- PubMed search for NCT04136041
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Smartphone Application
Trials testing the same drug.
- NCT07167654 — Smartphone Application to Support Mothers at Risk of Postpartum Depression · NA · active not recruiting
- NCT05169151 — Mobility and Physical Activity in Adolescent and Young Adult Cancer Patients or Survivors at Risk for Cardiovascular Mor · withdrawn
- NCT04263974 — Effectiveness of an Exercise Program and Education Through a Mobile Application for the Management of Patients With Hand · NA · completed
- NCT04192409 — Glycemic Control Using Mobile-based Intervention in Patients With Diabetes Undergoing Coronary Artery Bypass to Promote · NA · completed
- NCT03110016 — Smartphone Intervention for Subthreshold Depression · NA · completed
Other recruiting trials for Subthreshold Depression
Currently open trials in the same condition.
- NCT07319143 — The Effect of Transcranial Direct Current Stimulation (tDCS) in Improving Emotion Health · NA · recruiting
Other Kibi International University trials
Trials by the same sponsor.
- NCT03864484 — iPad Application-based Intervention for Post-stroke Depression · NA · unknown
- NCT03546218 — Effect of Positive-word Stimuli on the Limits of Stability During Multi-direction Reach Operation in Standing Position · NA · completed
- NCT03110016 — Smartphone Intervention for Subthreshold Depression · NA · completed
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 NCT04136041 (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 Kibi International University
- Last refreshed: 1 April 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/NCT04136041.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing