Skip to content

Delivery Pain and Postpartum Comfort

Effects of Acupressure and Shower Applied in the Delivery on the Intensity of Labor Pain and Postpartum Comfort

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04977713
Enrollment
120
Registered
2021-07-27
Start date
2019-05-15
Completion date
2020-01-31
Last updated
2021-07-27

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

Conditions

Acupressure, Hydrotherapy, Labor Pain, Postpartum Period

Keywords

labor pain, shower, acupressure, midwife, postpartum comfort

Brief summary

In this study was aimed that acupressure applied on the BL32 point and shower application reduced the intensity of labor pain experienced by the pregnant women in the active phase of labor and increased their postpartum comfort

Detailed description

Acupressure and shower are methods that can help reduce pain severity. This study thus aims to determine the effects of acupressure and shower on labour pain and postpartum comfort. This study was a randomized controlled trial (RCT). This study was the control group consisted of 40 pregnant women, while the experimental groups (acupressure and shower) consisted of 80 pregnant women in total. The experimental groups received routine labour care and either acupressure or showers upon reaching three cervical dilations (4-5, 6-7 and 8-10 cm). The control group only received routine labour care. A maternal information form (MIF), the Visual Analog Scale for Pain (VASP) and the Postpartum Comfort Questionnaire (PPCQ) were used to collect data. CONSORT checklist was used to report the current study.

Interventions

OTHERAcupressure

A researcher sat behind the women to comfortably access the sacral area and be in the appropriate position. The researcher then applied deep rotational pressure on the BL32 points until her nail bed colour changed to prevent any discomfort in the participants

OTHERShower

During uterine contractions, these participants took a shower while standing, with a researcher on hand to assist her (average time: 20 minutes). The water's temperature was between 22°C and 26°C.

Sponsors

Kırklareli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The randomized controlled trial

Eligibility

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

Inclusion criteria

* The inclusion criteria were being 20-40 years of age; * Having a foetus in vertex presentation * Having a foetus weighing 2.5-4 kg, as determined through ultrasonography * Being primiparous * Being between 37 and 42 gestational weeks with a single foetus * Having planned to have a spontaneous vaginal delivery * Not having used nonpharmacological pain control methods previously * Having a cervical dilation less than 5 cm (Dabiri et al., 2014) * Not having received analgesia or anaesthesia.

Exclusion criteria

* Were having a systemic disease during pregnancy (gestational diabetes, hypertension) * Taking medication regularly * Having a problem that prevented the woman from communicating * Undergoing psychiatric treatment (pharmacotherapy or psychotherapy) * Requiring an operative vaginal delivery (forceps, vacuum) * Receiving pharmacological interventions for labour pain.

Design outcomes

Primary

MeasureTime frameDescription
Reduce labor painEvaluation was done until delivery (on average between 8-12 hours)The participants were applicated acupressure, and shower as for birth pain. Pain has been evaluated with VASP.
Postpartum comfort levels2 hours after birthPostpartum comfort levels of the groups who received acupressure and shower in the postpartum period were evaluated.Postpartum comfort level has been evaluated with PPCQ.
A maternal information formbefore birthThis form consisted of 13 items asking for the participants' sociodemographic characteristics
Visual Analog Scale for Pain (VASP)Evaluation was done until delivery (on average between 8-12 hours)This scale is a 0-10 cm ruler developed by Bond and Pilowsky (Hawker et al., 2011; Aslan and Öztürk, 2014; Kömürcü and Ergin, 2014; Bond and Pilowsky, 1996). VASP is a 10 cm ruler which assessment with no pain at one end and worst pain at the other end. A Turkish validity and reliability study of the VASP was performed by Aslan and Öztürk (Aslan and Öztürk, 2014; Kömürcü and Ergin, 2014; Aslan, 2004).
Postpartum Comfort Questionnaire (PPCQ)2 hours after birthThe 48-item General Comfort Scale, developed by Kolcaba (Kolcaba, 1994), was first adapted into Turkish in 2008 by Kuğuoğlu and Karabacak, who also conducted a Turkish validity and reliability study on the scale (Kuğuoğlu and Karabacak, 2008). Based on the Turkish version of the GCS, Karakaplan and Yıldız (Karakaplan and Yıldız, 2010) developed the PPCQ. The PPCQ is a 5-point questionnaire with 34 items. Participants give items between 1 (strongly agree) and 5 points (strongly disagree). The lowest score possible is 34, and the highest score is 170, with higher scores indicating higher comfort levels.
Evalution labour painEvaluation was done until delivery (on average between 8-12 hours)VASP was evaluated before and after acupressure and shower applications.
Evalution postpartum comfort2 hours after birthPostpartum Comfort levels were evaluated in the postpartum period.

Countries

Turkey (Türkiye)

Outcome results

None listed

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