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Pilot Study clinical trials

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NCT ID: NCT05480423 Completed - Pilot Study Clinical Trials

Online Mindfulness-based Intervention on Parents of Children With Attention Deficit/Hyperactivity Disorder

ADHDparent
Start date: August 15, 2022
Phase: N/A
Study type: Interventional

This project apply curriculum of online programme materials and structure for mindful parenting and caregiving. It will include four modules (introductory mindfulness, mindful parenting, applying mindfulness in challenging moments, and advanced exercises for parents of children with special needs). Each module will include short psychoeducation videos and audio mindfulness exercises that can be used in various web-based or application-based platforms. A set of videos and audio exercises will be produced for the core program materials. One study of online mindful parenting program reported a low completion rate below 30%, showing the significance of weekly video or phone contact by professionals in program engagement. Although web-based or application-based mindfulness intervention have become popular, very limited effort has been developed for applying mindfulness in parenting and caregiving using technology. Only two published studies on online mindfulness-based intervention for parents are identified. Objectives of the study are: 1. Investigate the effects of online mindfulness-based intervention for parents of children with Attention Deficit/Hyperactivity Disorder. 2. Validate the protocol of the programme and explore the needs to make refinements of the programme based on the quantitative outcome and qualitative interview analyses

NCT ID: NCT04310995 Completed - Clinical trials for Coronary Artery Bypass Graft

Different Anti-Spastic Therapy Strategies After CABG Using Radial Artery Grafts

ASRAB-Pilot
Start date: June 2, 2020
Phase: Phase 4
Study type: Interventional

The Pilot study will be a single-center, randomized, open-label, active-controlled trial. After CABG surgery using Radial Artery Grafts (RA-CABG) and signing the informed consent, all patients will be screened according to the inclusion and exclusion criteria. Estimated 150 patients will be enrolled and randomized by ratio 1:1:1 to receive either Nicorandil (5mg tid po) or Diltiazem (180mg qd po) or Isosorbide Mononitrate (50mg qd po). Follow-up visits will be conducted at Week 1, 4, 12, and 24 after surgery. The last evaluation of study endpoints and other adverse events will be at Week 24. The pilot study is designed to explore the angiography outcomes of grafts and cardiovascular outcomes of patients, as well as safety outcomes among different anti-spastic regimens after RA-CABG.

NCT ID: NCT01437033 Completed - Human Volunteers Clinical Trials

Breath Test for Chemicals (Volatile Organic Compounds)

Start date: August 29, 2011
Phase:
Study type: Observational

Background: - Some types of cancer, like cancer of the esophagus, are difficult to detect at an early stage. A possible detection method involves collecting breath samples to look for chemicals that may be signs of cancer. However, more research is needed to determine how different chemicals appear in different breath samples. This study will involve healthy volunteers. Objectives: - To study chemicals appearing in breath samples of healthy volunteers. Eligibility: - Healthy volunteers between 30 and 60 years of age. Design: - Participants will fast overnight (midnight to morning) and then provide two breath samples taken 5 minutes apart. - Breath samples will be collected on days 1, 49, and 98 of the study

NCT ID: NCT01175161 Completed - Contraception Clinical Trials

Postpartum Intrauterine Device Study

PPIUD
Start date: October 2010
Phase: N/A
Study type: Interventional

The purpose of this non-blinded randomized clinical trial is to pilot the design of a randomized clinical trial to be conducted in Malawi to investigate immediate postpartum insertion of the Copper T380 intrauterine contraceptive device (CuT380A-IUCD) compared to placement at the 6-week postpartum visit. The investigators hypothesize that it will be feasible to enroll 140 women into this study, and that women will find the 10 minute to 48 hour time frame for IUCD placement acceptable.