New York, NY—November 19, 2014
A study at Hospital for Special Surgery (HSS) finds that a support group addressing the psychological and educational needs of people recently diagnosed with rheumatoid arthritis (RA) has a strong positive impact on their lives.
The study, titled, “Measuring the Impact of an Early RA Support and Education Program Using a Program Evaluation with Patient-Identified Outcomes,” will be presented in the ”Innovations in Rheumatologic Care” session at the American College of Rheumatology annual meeting on November 19 in Boston.
“The Early RA Support and Education program, a part of the Early Arthritis Initiative at Hospital for Special Surgery, addresses the unique psycho-educational needs of people recently diagnosed with rheumatoid arthritis,” said Adena Batterman, LCSW, manager of RA Support and Education Programs at HSS. “When developing the program, it was important that the patients’ voice and perspective were being considered in how we identified and addressed the specific needs of participants. To ensure this, we obtained patient feedback from many sources, which included focus groups.”
The free monthly program is the only one of its kind in the New York metropolitan area. Led by a clinical social worker and a rheumatology nurse manager, the program is open to anyone diagnosed with RA within the past two years. The meetings feature a lecture on topics of interest to RA patients, followed by a support group aimed at enhancing emotional coping and disease management strategies. The program is also part of Hospital for Special Surgery’s Community Service Plan.
“A diagnosis of rheumatoid arthritis is overwhelming and extremely stressful, so emotional and educational support are very important,” said Ted Fields, M.D., clinical director, Early Arthritis Initiative, Inflammatory Arthritis Center at HSS. “Meeting others with the same illness gives participants a sense of community and has a positive psychological impact. We also know that educated patients are more likely to stay on their medications, which is important in controlling RA.”
To evaluate the program’s impact, researchers designed a questionnaire to collect data in three key categories: “Managing RA,” “Connecting with Others with RA,” and “Coping with the Emotional Impact of RA.”
The 20 -item questionnaire uses multiple choice and open-ended questions to measure the program’s impact on patient-identified outcomes in each category. Support group participants received the questionnaire after each of 12 sessions between March 2013 and June 2014.
Researchers compiled results based on 127 questionnaires they got back from participants. Ninety-three percent of respondents were female, with a mean age of 49 (age range was 25 to 85). Ninety-two percent of participants had attended college.
In the questionnaire, respondents indicated how strongly they agreed or disagreed with statements related to managing their disease, coping, and connecting with others. Researchers noted several findings of interest.
In the “Managing RA” category, 90 percent of participants indicated that as a result of the session, they could make informed choices about their RA, and 84 percent felt that they were more prepared to discuss their RA treatment with their doctor.
In the category, “Connecting with Others,” 77 percent of participants indicated that speaking with other group members, they felt more hopeful about their RA, and 89 percent agreed that sharing information and feelings in the group helped them cope with RA.
In the “Emotional Impact” category, 79 percent of respondents indicated that participating in the program made them feel more confident in managing their RA and 61 percent said their RA was less disruptive to their daily life than it had been previously.
Responses to open-ended questions also supported the program’s value within the three categories. Patient comments included the following: ”I will follow up with MD about what I learned”; “I don’t feel so alone”; “I learned ways to deal with stress of RA”; “I know now where to find answers, feel empowered.”
Overall, the evaluation results indicate that the program is making a strong positive impact, according to researchers. In the “Emotional Impact” category, “RA is less disruptive to my daily life,” researchers noted that the results reflect a positive impact, though not as marked as in the other questions.
“Future work is needed to explore how patients define ‘disruptive’ to develop targeted content to address this for future groups. Additional research might also follow participants to determine how program participation over time and other variables affect this outcome,” Batterman said.
“We believe our process can serve as a model for including the patient perspective in evaluating outcomes in other disease-specific support and education programs,” she added.
American College of Rheumatology Meeting
“Measuring the Impact of an Early RA Support and Education Program Using a Program Evaluation with Patient Identified Outcomes,”
Presenter: Adena Batterman, LCSW, Manager of RA Support and Education Programs,
Department Social Work Programs, Hospital for Special Surgery
Authors: Adena Batterman, MSW, LCSW; Kathryn Klingenstein; Roberta Horton, LCSW, ACSW; Linda Leff, RN; Theodore R. Fields, MD; and Vivian P. Bykerk, MD. All from Hospital for Special Surgery.
Date: Wednesday, November 19, 2014
Oral presentation: 9:00 am – 10:30 am
Location: Exhibit Center, 259-A
Disclosure: A. Batterman, None; K. Klingenstein, None; R. Horton, None; L. Leff,
None; T. R. Fields, Pfizer Pharmaceuticals, 8; V. P. Bykerk, None.