Other Clinical Trial - A Multiple Baseline Design Study to Investigate

See also
Status	Clinical Trial	Phase
Completed	`NCT06390072` - Project Hypnos: The Impact of a Brief Hypnosis Intervention on Single-limb Dynamic Balance in People With Chronic Ankle Instability	N/A
Completed	`NCT02673658` - Project for Cognitive Advancement in Infants With Neuromotor Disorders	N/A
Completed	`NCT06125613` - Influence of Kinesiophobia on the Excitability of Connections Parieto-frontal During a Pointing Movement in Humans	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT06390072 - Project Hypnos: The Impact of a Brief Hypnosis Intervention on Single-limb Dynamic Balance in People With Chronic Ankle Instability

N/A

Completed

NCT02673658 - Project for Cognitive Advancement in Infants With Neuromotor Disorders

N/A

Completed

NCT06125613 - Influence of Kinesiophobia on the Excitability of Connections Parieto-frontal During a Pointing Movement in Humans

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03355417
Study type	Interventional
Source	Virginia Commonwealth University
Contact
Status	Completed
Phase	N/A
Start date	March 12, 2018
Completion date	March 20, 2019

A Multiple Baseline Design Study to Investigate the Effectiveness of OT-SI Using an Intensive Intervention Model

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms