The Social Life of Health Information

The Impact of Online Health Resources

About one in ten online health inquiries have a major impact on someone’s health care or the way they care for someone else.

When asked, “Did the health information you found in the last time online have a major impact on your own health care or the way you care for someone else, a minor impact, or no impact at all?”

  • 13% of e-patients say their most recent inquiry had a major impact.
  • 44% of e-patients say it had a minor impact.
  • 41% of e-patients say their most recent inquiry had no impact.

There are no differences between men and women or among age groups when it comes to the impact of online health inquiries. African American e-patients are more likely than white or Latino e-patients to report that their last online health session had a major impact (26%, compared with 11% and 16%). Seventeen percent of e-patients who report their health status as excellent or good say their most recent online health inquiry had a major impact, compared with 6% of those who report being in fair or poor health.

For the 57% of e-patients who say their most recent search had an impact, either major or minor:

  • 60% say the information found online affected a decision about how to treat an illness or condition.
  • 56% say it changed their overall approach to maintaining their health or the health of someone they help take care of.
  • 53% say it lead them to ask a doctor new questions, or to get a second opinion from another doctor.
  • 49% say it changed the way they think about diet, exercise, or stress management.
  • 38% say it affected a decision about whether to see a doctor.
  • 38% say it changed the way they cope with a chronic condition or manage pain.

The Center for Studying Health System Change’s large survey sample of 18,000 respondents afforded an opportunity to look closely at the impact of health information searches. Their data showed that African American and Latino information seekers were more likely than whites to say that “the information had a beneficial impact on their knowledge about treating an illness or condition.”21 Further study is needed to determine the reasons, but one factor cited by the study’s authors is that African American and Latino consumers are less likely than whites to have a usual doctor or other care provider and therefore “may find information obtained from other sources has more impact on their health knowledge or behaviors.” The Pew Hispanic Center and Robert Wood Johnson Foundation have also recorded lower levels of access to usual health care providers among Latinos in the U.S.22

Notes

21 Tu and Cohen, 2008

22 Gretchen Livingston, Susan Minushkin, and D'Vera Cohn, “Hispanics and Health Care in the United States: Access, Information and Knowledge.” (Pew Hispanic Center and Robert Wood Johnson Foundation: August 13, 2008) See: http://pewhispanic.org/reports/report.php?ReportID=91

Pew Internet Logo

Copyright 2012 Pew Internet & American Life Project

The Pew Research Center's Internet & American Life Project is one of seven projects that make up the Pew Research Center. The Center is supported by The Pew Charitable Trust.