Skip to content

Auricular acupuncture for treatment of low back pain and posterior pelvic pain in pregnancy

Auricular acupuncture for treatment of low back pain (LBP) and posterior pelvic pain in pregnancy in primary care: study protocol for a multicentre randomised placebo-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN41033073
Enrollment
212
Registered
2014-03-20
Start date
2014-02-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower back pain and/or pain in the posterior pelvic girdle Pregnancy and Childbirth

Interventions

A 4-hour workshop will be organised for all the midwives participating in the study, to demonstrate the implementation of the technique, the obstetric care to be provided and the study records to be k

Sponsors

Spanish Ministry of Health and Consumer Affairs (Carlos III Health Institute) (Spain)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Pregnant women (24 -36 weeks' gestation) 2. Aged at least 17 years 3. Diagnosed with pregnancy-related lower back pain and/or pain in the posterior pelvic girdle (LBPGP) 4. Who have not previously received acupuncture

Exclusion criteria

Exclusion criteria: 1. Pregnant women who began to suffer LBPGP before their pregnancy 2. Pregnant women with signs suggesting LBPGP secondary to inflammatory, infectious, traumatic, neoplastic or degenerative processes 3. Pregnant women receiving anticoagulation therapy or presenting dermatitis of the auricle

Design outcomes

Primary

MeasureTime frame
Reduction in pain intensity, according to the visual analogue scale (painVAS), at 2 weeks after the start of treatment.

Secondary

MeasureTime frame
1. Functional status with respect to LBPGP (according to the Roland-Morris lumbar disability questionnaire) 2. Health-related quality of life (SF12) at 2 weeks after the start of treatment 3. Reduction in pain intensity, according to the visual analogue scale (painVAS), at 12 and 48 weeks postpartum

Countries

Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 7, 2026