TY - JOUR
T1 - Community-based exercise (ComEx Pain) for older adults with chronic musculoskeletal pain: a protocol for a randomised controlled feasibility trial
AU - Conneely, Mairéad
AU - Sullivan, Kieran O’
AU - Ryan, Cormac
AU - Clifford, Amanda
AU - Coote, Susan
AU - Eshghimanesh, Zohreh
AU - Sullivan, Vincent O’
AU - Robinson, Katie
AU - Shiely, Frances
AU - Glynn, Liam
AU - Woods, Catherine
AU - Harmon, Dominic
AU - Macken, Phelim
AU - Meaney, Ryan
AU - Phelan, Martina
AU - Centre, Public and Patient Involvement Panel of Aging Research
AU - McCreesh, Karen
PY - 2024/11/15
Y1 - 2024/11/15
N2 - Background Chronic musculoskeletal pain is a key societal challenge in Ireland, affecting one in three adults over the age of 50, with societal and healthcare costs of over €5.34 billion per year. Physical activity can form a key part of the management of people living with chronic pain, along with providing a myriad of health-enhancing and disease-prevention benefits for older adults. However, pain can limit engagement in physical activity, leading to the negative effects of chronic pain in older adults. Public and Patient involvement in this study identified that people with chronic pain fear exacerbation of their symptoms with exercise, and value having an experienced exercise leader who understands their needs. The primary aim of this study was to examine the feasibility and acceptability of a community-based exercise intervention, ComEx Pain, specifically tailored to older adults with chronic musculoskeletal pain. This paper reports a protocol designed to evaluate the feasibility of conducting a two-arm randomized controlled trial (RCT). Methods ComEx Pain is a randomised controlled feasibility trial with embedded economic and process evaluations. Community-dwelling adults aged ≥50 years living with chronic musculoskeletal pain will be recruited in the mid-western region of Ireland. Randomisation will be conducted using a 1:1 allocation ratio into two groups: (1) an intervention group receiving a community-based exercise program led by trainers educated in supporting people with chronic pain and (2) a control group who will receive a paper-based education manual. Primary outcomes for feasibility include recruitment rate, retention rate, and adherence to the intervention. The secondary outcomes will include changes in pain, physical function, emotional function, and physical activity. Discussion If this pilot feasibility study finds evidence to support feasibility and acceptability, a future larger-scale definitive trial will be conducted to examine the effectiveness of ComEx Pain in older adults living with chronic musculoskeletal pain. Trial registration number: Registered at Clinical Trials.gov NCT06535633.
AB - Background Chronic musculoskeletal pain is a key societal challenge in Ireland, affecting one in three adults over the age of 50, with societal and healthcare costs of over €5.34 billion per year. Physical activity can form a key part of the management of people living with chronic pain, along with providing a myriad of health-enhancing and disease-prevention benefits for older adults. However, pain can limit engagement in physical activity, leading to the negative effects of chronic pain in older adults. Public and Patient involvement in this study identified that people with chronic pain fear exacerbation of their symptoms with exercise, and value having an experienced exercise leader who understands their needs. The primary aim of this study was to examine the feasibility and acceptability of a community-based exercise intervention, ComEx Pain, specifically tailored to older adults with chronic musculoskeletal pain. This paper reports a protocol designed to evaluate the feasibility of conducting a two-arm randomized controlled trial (RCT). Methods ComEx Pain is a randomised controlled feasibility trial with embedded economic and process evaluations. Community-dwelling adults aged ≥50 years living with chronic musculoskeletal pain will be recruited in the mid-western region of Ireland. Randomisation will be conducted using a 1:1 allocation ratio into two groups: (1) an intervention group receiving a community-based exercise program led by trainers educated in supporting people with chronic pain and (2) a control group who will receive a paper-based education manual. Primary outcomes for feasibility include recruitment rate, retention rate, and adherence to the intervention. The secondary outcomes will include changes in pain, physical function, emotional function, and physical activity. Discussion If this pilot feasibility study finds evidence to support feasibility and acceptability, a future larger-scale definitive trial will be conducted to examine the effectiveness of ComEx Pain in older adults living with chronic musculoskeletal pain. Trial registration number: Registered at Clinical Trials.gov NCT06535633.
UR - http://dx.doi.org/10.12688/hrbopenres.13981.1
U2 - 10.12688/hrbopenres.13981.1
DO - 10.12688/hrbopenres.13981.1
M3 - Article
SN - 2515-4826
JO - HRB Open Research
JF - HRB Open Research
ER -