The Use of Implementation Intentions to Increase the Appointment Attendance of OEF/OIF Veterans
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01649934|
Recruitment Status : Recruiting
First Posted : July 25, 2012
Last Update Posted : March 27, 2017
|Condition or disease||Intervention/treatment||Phase|
|Brain Injuries||Behavioral: Implementation Intention Behavioral: Contact Clinic||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||60 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||The Use of Implementation Intentions to Increase the Appointment Attendance of Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) Veterans|
|Study Start Date :||June 2013|
|Estimated Primary Completion Date :||December 2017|
|Estimated Study Completion Date :||December 2017|
No Intervention: Scheduling as Usual
Participants will be subject to the current appointment scheduling procedures.
Experimental: Contact Clinic
This group will be required to contact the clinic themselves to make appointments.
Behavioral: Contact Clinic
Participants will be asked to sign a form indicating their need to contact the recommended clinics to make their appointments.
Experimental: Implementation Intentions
This group will create Implementation Intentions to contact the clinic to make their appointments and to attend those appointments.
Behavioral: Implementation Intention
Implementation Intentions are a series of what/when/where statements that a participant will make to create automatic cues to complete a behaviorally advantageous action.
- Attendance at Scheduled Appointments [ Time Frame: Over a 60 Day Period ]The attendance of the participants at their scheduled appointments will be measured.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01649934
|Contact: Joseph F Kulas, Ph.D.||203-932-5711 ext email@example.com|
|United States, Connecticut|
|VA Connecticut Healthcare System||Recruiting|
|West Haven, Connecticut, United States, 06516|
|Principal Investigator: Joseph F Kulas, Ph.D.|
|Principal Investigator:||Joseph F Kulas, Ph.D.||VA Connecticut Healthcare System|