TY - JOUR
T1 - Nonsurgical management of hallux valgus
T2 - findings of a randomised pilot and feasibility trial
AU - Menz, Hylton B.
AU - Lim, Polly Q.X.
AU - Hurn, Sheree E.
AU - Mickle, Karen J.
AU - Buldt, Andrew K.
AU - Cotchett, Matthew P.
AU - Roddy, Edward
AU - Wluka, Anita E.
AU - Erbas, Bircan
AU - Batra, Mehak
AU - Munteanu, Shannon E.
N1 - Funding Information:
This study was funded by the La Trobe University Research Focus Area in Sport, Exercise and Rehabilitation Grant-ready Scheme. The footwear was provided at a discounted cost by Global Footcare (Coomera, Queensland, Australia) and the foot orthoses were donated by Foot Science International (Christchurch, New Zealand). The funders were not involved in the design of the study, in the writing of the protocol, or in the decision to submit the manuscript for publication.
Funding Information:
HBM was a National Health and Medical Research Council (NHMRC) Senior Research Fellow (ID: 1135995) when this trial was undertaken. We would like to acknowledge the support of Jeff Coombridge (Global Footcare, Coomera, Queensland, Australia) and Steve Lafferty (Foot Science International, Christchurch, New Zealand).
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/11/13
Y1 - 2023/11/13
N2 - Background: Hallux valgus is a common and disabling condition. This randomised pilot and feasibility trial aimed to determine the feasibility of conducting a parallel group randomised trial to evaluate the effectiveness of a nonsurgical intervention for reducing pain associated with hallux valgus. Methods: Twenty-eight community-dwelling women with painful hallux valgus were randomised to receive either a multifaceted, nonsurgical intervention (footwear, foot orthoses, foot exercises, advice, and self-management) or usual care (advice and self-management alone). Outcome measures were obtained at baseline, 4, 8 and 12 weeks. The primary outcome was feasibility, evaluated according to demand (recruitment rate and conversion rate), acceptability, adherence, adverse events, and retention rate. Limited efficacy testing was conducted on secondary outcome measures including foot pain, foot muscle strength, general health-related quality of life, use of cointerventions, and participants’ perception of overall treatment effect. Results: Between July 8, 2021, and April 22, 2022, we recruited and tested 28 participants (aged 44 to 80 years, mean 60.7, standard deviation 10.7). This period encompassed two COVID-related stay-at-home orders (July 16 to July 27, and August 5 to October 21, 2021). The predetermined feasibility thresholds were met for retention rate, foot pain, mental health-related quality of life, and use of cointerventions, partly met for acceptability, adverse events, and muscle strength, and not met for demand (recruitment rate or conversion rate), adherence, physical health-related quality of life and perception of overall treatment effect. Conclusion: In its current form, a randomised trial of footwear, foot orthoses, foot exercises, advice and self-management for relieving pain associated with hallux valgus is not feasible, particularly due to the low adherence with the intervention. However, it is difficult to determine whether the trial would be feasible under different circumstances, particularly due to COVID-19 stay-at-home orders. Future trials will need to consider improving the aesthetics of the footwear and making the exercise program less burdensome. Trial registration: Australian and New Zealand Clinical Trial Registry (ACTRN12621000645853).
AB - Background: Hallux valgus is a common and disabling condition. This randomised pilot and feasibility trial aimed to determine the feasibility of conducting a parallel group randomised trial to evaluate the effectiveness of a nonsurgical intervention for reducing pain associated with hallux valgus. Methods: Twenty-eight community-dwelling women with painful hallux valgus were randomised to receive either a multifaceted, nonsurgical intervention (footwear, foot orthoses, foot exercises, advice, and self-management) or usual care (advice and self-management alone). Outcome measures were obtained at baseline, 4, 8 and 12 weeks. The primary outcome was feasibility, evaluated according to demand (recruitment rate and conversion rate), acceptability, adherence, adverse events, and retention rate. Limited efficacy testing was conducted on secondary outcome measures including foot pain, foot muscle strength, general health-related quality of life, use of cointerventions, and participants’ perception of overall treatment effect. Results: Between July 8, 2021, and April 22, 2022, we recruited and tested 28 participants (aged 44 to 80 years, mean 60.7, standard deviation 10.7). This period encompassed two COVID-related stay-at-home orders (July 16 to July 27, and August 5 to October 21, 2021). The predetermined feasibility thresholds were met for retention rate, foot pain, mental health-related quality of life, and use of cointerventions, partly met for acceptability, adverse events, and muscle strength, and not met for demand (recruitment rate or conversion rate), adherence, physical health-related quality of life and perception of overall treatment effect. Conclusion: In its current form, a randomised trial of footwear, foot orthoses, foot exercises, advice and self-management for relieving pain associated with hallux valgus is not feasible, particularly due to the low adherence with the intervention. However, it is difficult to determine whether the trial would be feasible under different circumstances, particularly due to COVID-19 stay-at-home orders. Future trials will need to consider improving the aesthetics of the footwear and making the exercise program less burdensome. Trial registration: Australian and New Zealand Clinical Trial Registry (ACTRN12621000645853).
UR - http://www.scopus.com/inward/record.url?scp=85176339206&partnerID=8YFLogxK
U2 - 10.1186/s13047-023-00677-1
DO - 10.1186/s13047-023-00677-1
M3 - Article
C2 - 37957676
AN - SCOPUS:85176339206
SN - 1757-1146
VL - 16
JO - Journal of Foot and Ankle Research
JF - Journal of Foot and Ankle Research
IS - 1
M1 - 78
ER -