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Published on: March 1, 2024
Supervised, Individualised Exercise Across Pregnancy and Postpartum for Pregnancy-Related Lumbopelvic Pain: A
Keiichi Oishi1,2, Jota Maki3,4, Tomohiro Mitoma3,5
1Department of Obstetrics and Gynecology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Kita-ku, Okayama, Japan.
Objective:
To evaluate the effectiveness of a face-to-face supervised, individualised exercise programme and pelvic belt in women with pregnancy-related low back and pelvic girdle pain (PLBP/PPGP) from pregnancy through the postpartum period.
Design:
Multicentre, non-randomised, site-allocated pragmatic cluster trial.
Setting:
Tertiary care hospitals and obstetrics and gynaecology clinics.
Population:
Pregnant women with PLBP/PPGP at ≥ 28 weeks' gestation.
Methods:
Participants were allocated by study site to one of three groups: (1) leaflet; (2) exercise; (3) exercise plus belt. All groups received exercise leaflets. The exercise and exercise plus belt groups received three 30-min, face-to-face, supervised sessions-during late pregnancy, 5 days postpartum, and 1 month postpartum. The exercise plus belt group additionally received a pelvic belt.
Main Outcome Measures:
Functional impairment was assessed by the Oswestry Disability Index (ODI) at 5 days, 1 month, and 3 months postpartum.
Results:
A total of 127 participants were enrolled; 107 completed follow-up. At 1 month postpartum, lower ODI scores were observed in the exercise group (mean difference 5.4; 95% CI 3.3 to 7.6), and similarly in the exercise plus belt group (mean difference 4.9; 95% CI 2.6 to 7.2), compared with the leaflet group. At 3 months postpartum, mean differences were 4.4 (95% CI -7.1 to 15.9) for the exercise group and 3.7 (95% CI -7.9 to 15.2) for the exercise plus belt group. No clear differences were observed between the exercise and exercise plus belt groups.
Conclusions:
A face-to-face supervised, individualised exercise programme was associated with lower functional impairment at 1 month postpartum.
Trial Registration:
UMIN Clinical Trials Registry (UMIN000057866); https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066135.
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