Abstract: Using Webex Technology to Increase Knowledge and Awareness about Multiple Sclerosis Via Documentary Film and Panel As an Educational Intervention (Society for Social Work and Research 26th Annual Conference - Social Work Science for Racial, Social, and Political Justice)

712P Using Webex Technology to Increase Knowledge and Awareness about Multiple Sclerosis Via Documentary Film and Panel As an Educational Intervention

Schedule:
Sunday, January 16, 2022
Marquis BR Salon 6, ML 2 (Marriott Marquis Washington, DC)
* noted as presenting author
Boyd Suzanne, Associate Professor Social Work, University of North Carolina at Charlotte, Charlotte, NC
Shelby Veri, Health Services Research Doctoral Candidate, University of North Carolina at Charlotte, NC
Background and Primary Purpose. Multiple Sclerosis (MS) is an autoimmune disease with no known cure that attacks the protective coverings of nerves which results in a communication malfunction between the body and central nervous system. Common symptoms include numbness, fatigue, impaired coordination, muscle spasms. 1 million adults live with MS in the US, yet knowledge and awareness about MS among social workers and the general public is very limited. Study objectives: (1) increase knowledge and awareness about MS through use of documentary film and panel discussion using WebEx technology in the University/local community and (2) increase awareness of national, state, and local MS resources.

Methods. A pre-experimental, posttest only design assessed the impact of using WebEx technology to increase knowledge and awareness about MS and available resources to a University/Charlotte community. WebEx is an on-line video conferencing technology used to conduct on-line meetings/webinars. Participants viewed a 2019 documentary film, “When We Walk,” about a filmmaker’s personal experience with primary progressive MS, followed by a 30 minute virtual panel discussion (persons living with MS, a NMSS MS Navigator Program representative, UNC Charlotte ADA Coordinator, Physician Assistant/MSW provider). Participants posted questions in the chat function during the event. Nineteen of the 29 participants (65.5%) completed a confidential 24-item post-event electronic survey (via Qualtrics). The majority of participants were female (n=17; 89.47%) and between the ages of 45 to 64 years old (n=13; 68.52%). Participants included 3 persons of color (Hispanic/Latino; Black/African American; African) (16.66%), 14 Caucasians (77.78%), and 1 other ethnicity (5.56%). Participants were highly educated: trade/technical/vocational training (n=1), Associates degree (n=1), Bachelor's degree (n=6), Master’s degree (n=6), Doctoral or Professional degree (n=5).

Results. The findings reveal that 94.74% (n=18) participants “agreed” or “strongly agreed” that “participation in the MS documentary screening and panel discussion increased my knowledge of MS and its related symptomatology”. Eighteen participants (94.74%) “agreed” or “strongly agreed” “participation in the MS film screening and panel discussion increased my knowledge of available resources at UNC Charlotte and the surrounding area”. All participants “agreed” or “strongly agreed” that “the virtual event met my expectations”. Seventeen participants (94.44%) rated the “When We Walk” film screening and panel experience as “excellent.”

Implications. The findings demonstrate WebEx is an effective technology as is the use of documentary film and panel discussion to increase participant knowledge and awareness of MS and resources notably during the COVID-19 pandemic to promote inclusivity of various populations. Further community outreach efforts are needed to bring more MS education and resource awareness and ZOOM pop-up events to racial and ethnic minority populations, family members, and social workers. In an effort to achieve this goal the PI received funds to develop a MS 10 module training intervention with 8 students about MS and offering regular 30 minute ZOOM “MS Talks” pop-up events free to the general public to help them learn about MS and resources. Notably, social workers in the academy with expertise about MS is very limited and further educational efforts to change status is needed.