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Comparing Google With A Focused Diabetes Search Engine

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ClinicalTrials.gov Identifier: NCT01080976
Recruitment Status : Completed
First Posted : March 5, 2010
Results First Posted : February 7, 2018
Last Update Posted : February 7, 2018
Sponsor:
Information provided by (Responsible Party):
Charles Safran, Beth Israel Deaconess Medical Center

Study Type: Observational
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Condition: Diabetes

  Participant Flow

Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups
  Description
Primary Care Physicians No text entered.
Diabetologists No text entered.

Participant Flow:   Overall Study
    Primary Care Physicians   Diabetologists
STARTED   5   5 
COMPLETED   5   5 
NOT COMPLETED   0   0 



  Baseline Characteristics

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
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Reporting Groups
  Description
Primary Care Physicians No text entered.
Diabetologists No text entered.
Total Total of all reporting groups

Baseline Measures
   Primary Care Physicians   Diabetologists   Total 
Overall Participants Analyzed 
[Units: Participants]
 5   5   10 
Age 
[Units: Participants]
Count of Participants
     
<=18 years      0   0.0%      0   0.0%      0   0.0% 
Between 18 and 65 years      5 100.0%      5 100.0%      10 100.0% 
>=65 years      0   0.0%      0   0.0%      0   0.0% 
Sex: Female, Male 
[Units: Participants]
Count of Participants
     
Female      1  20.0%      2  40.0%      3  30.0% 
Male      4  80.0%      3  60.0%      7  70.0% 


  Outcome Measures

1.  Primary:   Website Ranking   [ Time Frame: Immediate ]

2.  Primary:   Search Engine Preference   [ Time Frame: Immediate ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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  More Information

Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.


Results Point of Contact:  
Name/Title: Charles Safran
Organization: BIDMC
phone: 617-278-8170
e-mail: csafran@bidmc.harvard.edu



Responsible Party: Charles Safran, Beth Israel Deaconess Medical Center
ClinicalTrials.gov Identifier: NCT01080976     History of Changes
Other Study ID Numbers: 2009P000356
First Submitted: March 3, 2010
First Posted: March 5, 2010
Results First Submitted: March 27, 2017
Results First Posted: February 7, 2018
Last Update Posted: February 7, 2018