NCT03685292

Brief Summary

The focus of this study is to evaluate whether a new fraud material will be suitable for a technological device and or software. \*\*\*For consultation purposes only.\*\*\*

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
37

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2018

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2018

Completed
29 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2018

Completed
12 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 12, 2018

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 19, 2018

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 26, 2018

Completed
Last Updated

September 26, 2018

Status Verified

July 1, 2018

Enrollment Period

29 days

First QC Date

July 19, 2018

Last Update Submit

September 21, 2018

Conditions

Outcome Measures

Primary Outcomes (1)

  • Questionnaire/Screening

    The tool, intended to assess college students' by classmates, includes one portion that is an online self-administered questionnaire. Guidance counselors can use the questionnaire to identify college students students who have been targeted for "Fraud."

    30 days

Study Arms (3)

Group A

Subject(s): A Subgroup

Behavioral: Behavioral Advisory SystemDrug: Behavioral TreatmentDevice: Behavioral Division

Group B

Subject(s): B Subgroup

Behavioral: Behavioral Advisory SystemDrug: Behavioral TreatmentDevice: Behavioral Division

Group C

Subject(s): C Sub Group

Behavioral: Behavioral Advisory SystemDrug: Behavioral TreatmentDevice: Behavioral Division

Interventions

Support and training to help increase throughput while promoting upstanding stature and reproducibility in behavioral testing using cutting edge methodologies.

Also known as: Triple Helix Methodology System
Group AGroup BGroup C

This study addressed the efficacy of cognitive-behavioral therapy (CBT) treatment.

Group AGroup BGroup C

This study is relative to minimal contact control (MCC).

Group AGroup BGroup C

Eligibility Criteria

Age19 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

African-American Cased-Based

You may qualify if:

  • College Student

You may not qualify if:

  • Age Over 40

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Southern University

Baton Rouge, Louisiana, 70807, United States

Location

Related Links

MeSH Terms

Conditions

Behavior

Interventions

Behavior Therapy

Intervention Hierarchy (Ancestors)

PsychotherapyBehavioral Disciplines and Activities

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Student

Study Record Dates

First Submitted

July 19, 2018

First Posted

September 26, 2018

Study Start

April 1, 2018

Primary Completion

April 30, 2018

Study Completion

May 12, 2018

Last Updated

September 26, 2018

Record last verified: 2018-07

Locations