Adherence, tolerance and effectiveness of two different pelvic support belts as a treatment for pregnancy-related symphyseal pain - a pilot randomized trial

• Published in: BMC pregnancy and childbirth Vol. 15; no. 1; p. 36
• Main Authors: Flack, Natasha A M S, Hay-Smith, E Jean C, Stringer, Mark D, Gray, Andrew R, Woodley, Stephanie J
• Format: Journal Article
• Language: English
• Published: England BioMed Central 15.02.2015; BioMed Central Ltd
• Subjects: Activities of Daily Living; Adult; Back pain; Biomechanics; Braces; Clinical trials; Evidence-based medicine; Female; Humans; Pain Management - instrumentation; Pain Management - methods; Pain Measurement; Patient Compliance; Patient Preference; Pelvic Girdle Pain - diagnosis; Pelvic Girdle Pain - etiology; Pelvic Girdle Pain - physiopathology; Pelvic Girdle Pain - therapy; Pregnancy; Pregnancy complications; Pregnancy Complications - diagnosis; Pregnancy Complications - etiology; Pregnancy Complications - physiopathology; Pregnancy Complications - therapy; Questionnaires; Text messaging; Treatment Outcome; Womens health; New Zealand
• ISSN: 1471-2393; 1471-2393
• DOI: 10.1186/s12884-015-0468-5

Pregnancy-related pubic symphysis pain is relatively common and can significantly interfere with daily activities. Physiotherapist-prescribed pelvic support belts are a treatment option, but little evidence exists to support their use. This pilot compared two pelvic belts to determine effectiveness (symptomatic relief), tolerance (comfort) and adherence (frequency, duration of use). Unblinded, 2-arm, single-center, randomized (1:1) parallel-group trial. Twenty pregnant women recruited from the community (Dunedin, New Zealand), with physiotherapist-diagnosed symphyseal pain, were randomly allocated to wear either a flexible or rigid belt for three weeks. One author, not involved in data collection, randomized the allocation to trial group. The unblinded primary outcome was the Patient Specific Functional Scale (PSFS). Secondary outcomes were pain intensity during the preceding 24 hours and preceding week (visual analogue scale [VAS]), and disability (Modified Oswestry Disability Questionnaire [MODQ]). Duration of use (hours) was recorded daily by text messaging. Participants were assessed at baseline, by weekly phone interviews and at intervention completion (three weeks). To assess comfort, women wore the alternate belt in the fourth week. Twenty pregnant women (mean ± SD age, 29.4 ± 6.5 years; mean gestation at baseline, 30.8 ± 5.2 weeks) were randomized to treatment groups (flexible = 10, rigid =10) and all were included in analysis. When adjusted for baseline, PSFS scores were not significantly different between groups at follow up (mean difference -0.1; 95% CI: -2.5 to 2.3; p =0.94). Pain in the preceding 24 hours reached statistical significance in favor of the flexible belt (VAS, p = 0.049). Combining both groups' data, function and pain were significantly improved at three weeks (mean difference -2.3; 95% CI: 1.2 to 3.5; p< 0.001). Belts were worn for an average of 4.9 ± 2.9 hours per day; women preferred the flexible belt. No adverse events were reported. These preliminary results suggest the flexible pelvic support belt may be more effective in reducing pain and is potentially better tolerated than a rigid belt. Based on these data, a larger trial is both feasible and clinically useful. Australian New Zealand Clinical Trials Registry (ANZCTR) ACTRN12614000898651 , 25th August, 2014.