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NCT06267534
Mindfulness-based Mobile Applications Program
NA trial testing mindfulness-based mobile applications program in COVID-19 in 102 participants. Completed in 22 September 2022.
22 September 2022
Quick facts
| Lead sponsor | Yu-Chien Huang |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | sequential |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 102 |
| Start date | 9 September 2022 |
| Primary completion | 22 September 2022 |
| Estimated completion | 22 September 2022 |
| Sites | 1 location across Taiwan |
Drugs / interventions tested
- mindfulness-based mobile applications program
Conditions studied
- COVID-19 — all drugs for COVID-19 →
- Cell Phone Use — all drugs for Cell Phone Use →
- Nurse — all drugs for Nurse →
- Mental Health — all drugs for Mental Health →
Sponsor
Yu-Chien Huang
Who can join
18 and older, any sex, with COVID-19 or Cell Phone Use. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this type of study: quasi-experimental clinical trial . The purpose of this study is to explore the effects of applying mindfulness-based mobile applications program to maintaining mental health of emergency nurses during providing care to COVID-19 patients. The main question\[s\] it aims to answer are: 1. To explore the effect of mindfulness-based mobile device-assisted program on care stress of emergency nurses caring for COVID-19 patients. 2. To explore the impact of mindfulness-based mobile device-assisted programs on the psychological distress of emergency nurses caring for COVID-19 patients. 3. To explore the impact of a mindfulness-based mobile device-assisted program on compassion fatigue in emergency nurses caring for COVID-19 patients. Participants will Mindfulness-based mobile device is provided to experimental group as assistance for 2 weeks. In the contrary, no intervention measure was assigned in the control group. Scale exam was performed before and after the program in both groups at the same time.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06267534
- Europe PMC full search
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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 NCT06267534 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Yu-Chien Huang
- Last refreshed: 20 February 2024
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/NCT06267534.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing