In 2010, about 1 in 3 adults who had seen a physician or other health care professional in the past year had been advised to begin to exercise or continue with their physical activity program, says a February 8 National Center for Health Statistics data brief. Furthermore, the percentage of adults who had been advised to exercise increased from 22.6% in 2000 to 32.4% in 2010.
Younger people were told to exercise more often than older adults in 2010. However, adults aged 18-24 had the smallest increase over the decade 2000-2010 in the percentage receiving a recommendation to exercise (from 10.4% in 2000 to 16.1% in 2010), while adults aged 85 and over had the largest percentage point increase (from 15.3% in 2000 to 28.9% in 2010). In addition, Hispanic adults had the largest percentage point increase over the decade 2000-2010 in receiving a recommendation to exercise.
Receiving advice to exercise varied with having selected chronic health conditions. Between 2000 and 2010, receipt of advice from a physician to exercise or engage in physical activity increased for adults with hypertension, cardiovascular disease, cancer, and diabetes. Adults with diabetes were more likely than those with hypertension, cardiovascular disease, or cancer to have been advised to exercise. In 2010, more than one-half of adults with diabetes were advised to exercise, compared with just over one-third of adults with cancer.
Adults who were obese were about twice as likely as healthy weight adults to have been advised by a physician or other health care professional to exercise. The percentage of adults who had been advised to exercise increased in each body mass index category (underweight, healthy weight, overweight, obese) between 2000 and 2010, although the percentage point increase was largest for adults who were obese.
A new committee appointed yesterday by the National Institutes of Health (NIH) will coordinate pain research activities across the federal government with the goals of stimulating pain research collaboration, fully leveraging the government resources dedicated to supporting pain research, and providing an important avenue for public involvement.
The Interagency Pain Research Coordinating Committee members include leading federal officials, including an individual from the Rehabilitation Research and Development Service at the Department of Veterans Affairs, Office of Research and Development; 6 nonfederal scientists; physicians; other health professionals; and 6 members of the general public who are representatives of leading research, advocacy, and service organizations. Appointees include organizations that advocate for people with fibromyalgia, chronic vulvar pain and related pain disorders, and peripheral neuropathies.
Created through the Affordable Care Act, the committee also will explore public-private partnerships to broaden collaborative, cross-cutting research, and consider best practices in disseminating information about pain to public and professional audiences.
Only through clinical research can the health care profession gain insights and answers about advancing prevention, treatments, and cures for disease and disability. To that end, the National Institutes of Health has compiled resources to raise awareness of the importance of clinical research and get the public to think about participating in clinical trials, including those involving physical therapy. Information for physical therapists and other health care providers includes opportunities for education and awareness; promotional posters, flyers, and slides; and guidance for talking with patients about, and referring them to, clinical trials.
A new report summarizes key issues and recommendations discussed at the Summit on The Value in Musculoskeletal Care, sponsored by the United States Bone and Joint Initiative (USBJI). The summit, held in Washington, DC, October 12-13, 2011, was attended by 127 invited representatives of the musculoskeletal community, including APTA staff and members, patients, health care professionals, payers, industry, and government.
Specifically, the report provides a definition of the value in musculoskeletal care, addresses the need for accurate and reliable measurements to assess quality and value of musculoskeletal care, outlines advocacy strategies, and makes recommendations on health organizations' roles in efforts to increase the value of musculoskeletal care.
According to USBJI, the report's proposals should meet several important goals to:
APTA is a founding member of USBJI. Member organizations are encouraged to consider strategic plans for collaborative implementation of the recommendations, in concert with USBJI and other groups.
Read summaries of the Pauline Cerasoli and Linda Crane lectures and learn about the implications of cardiac comorbidities in outpatient settings, use of red flags when assessing low back pain, benefits of aquatic physical therapy as a complement to land-based therapy, and more in the
February 11 issue
of CSM 2012 Daily News. The
issues also are available on the Combined Sections Meeting (CSM)
, and a final, digital "wrap-up" issue will be e-mailed to all members in the next 2 weeks.