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Pain Relief by Applying TENS on Acupuncture Points During the First Stage of Labour

Pain Relief by Applying Transcutaneous Electrical Nerve Stimulation (TENS) on Acupuncture Points During the First Stage of Labour: a Randomised Controlled Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00148577
Enrollment
100
Registered
2005-09-08
Start date
2002-08-31
Completion date
2003-12-31
Last updated
2005-09-08

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

Conditions

Pain Relief at First Stage

Keywords

Pain Relief, TENS, Acupuncture Points

Brief summary

We aimed to establish the reduction of labor pain by applying TENS at acupuncture points during the first stage of labour, to assess their efficacy, and to ascertain their acceptability.

Detailed description

We conducted a double-blind, placebo-controlled randomised trial involving healthy parturient at term pregnancy using TENS on 4 acupuncture points (Li 4 and Sp 6) (n=50) and the placebo group (n=50). Visual analogue scale (VAS) was used to assess the effect on pain before the application, 30 minutes and 60 minutes after TENS. The objective parameter of outcome was the score of VAS decreased in each groups. A post-partum questionnaire was given 24 hours later to evaluate the satisfaction and the use of this pain relieving method for the next delivery.

Interventions

DEVICETranscutaneous Electrical Nerve Stimulation

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

The inclusion criteria were: * Voluntary informed participation to the study * An initial wish to deliver without epidural analgesia * Planned vaginal childbirth (non-obstetrical complicated pregnancy) * Fetal vertex presentation * Term pregnancy (\>37 weeks of gestation) * Apply at 1st stage of labour and excluded if cervical dilatation \> 5 cm * Age between 20 and 40 years * Chinese speaking, capable to understand the study * No experience of pain relief by systemic or epidural anesthesia in previous delivery * No experience in acupuncture or TENS in other field * Had no heart disease nor using pace-maker.

Exclusion criteria

* Cervical dilatation \> 5 cm * Experience of pain relief by systemic or epidural anesthesia in previous delivery * Experience in acupuncture or TENS in other field * Had heart disease or using pace-maker

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026