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Acupressure and Comfort at Childbirth

The Impact of Applying Various Forms of Acupressure on Women's Hand During Labor on Their Childbirth Comfort: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05407103
Enrollment
129
Registered
2022-06-07
Start date
2020-08-24
Completion date
2022-02-21
Last updated
2022-06-07

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

Conditions

Pain, Labor

Keywords

Pain, Labor, Comfort

Brief summary

Aims: Non-pharmacological methods employed for management labor pain also help pregnant women to cope with labor pain and increase their childbirth comfort. The aim of this study is to determine the effect of cold and hot acupressure applications, applied to the acupressure point LI4 of primiparous women during labor, on their childbirth comfort. Methods: This study was designed a randomized controlled experimental study. The sample consisted of 129 healthy pregnant women including 44 pregnant women in the hot acupressure group, 44 pregnant women in the cold acupressure group, and 41 pregnant women in the control group. The Personal Information Form, the Labor Monitoring Form, the Visual Analog Scale, and the Childbirth Comfort Questionnaire were all used to gather the data.

Interventions

OTHERCold Acupressure

For the cold acupressure application, the researchers prepared pouches that were 3 cm long, 2 cm wide, and 1 cm high (3x2x1cm), and filled with cherry seeds - to retain heat for a longer time, hence the preference. Next, they fixed rubber bands to the pouches so that they stayed in place on the participants' hands during acupressure, and retain consistent pressure throughout. Lastly, the cold acupressure pouches were kept in a freezer for 40 minutes.

OTHERWarm Acupressure

For the warm acupressure application, the researchers prepared pouches that were 3 cm long, 2 cm wide, and 1 cm high (3x2x1cm), and filled with cherry seeds - to retain heat for a longer time, hence the preference. Next, they fixed rubber bands to the pouches so that they stayed in place on the participants' hands during acupressure, and retain consistent pressure throughout. Lastly, the warm acupressure pouches were heated in a microwave at 600 W for one minute.

Sponsors

Serap Ozturk Altinayak
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Being a primipara * Having intact membranes * No skin diseases (such as urticaria...), * No use of narcotic drugs * Having a term pregnancy * Having a single fetus at vertex position * Planning to have vaginal delivery * Having contractions and ongoing regular augmentation * Having recent augmentation starting periods * Being in the latent phase (0-3 cm dilatation) * Having no history of high-risk pregnancy * Not using analgesic drugs to reduce pain during delivery * Having no systemic and neurologic diseases * Having no contraction anomaly (hypotonic or hypertonic contractions)

Exclusion criteria

• Having any of the above criteria

Design outcomes

Primary

MeasureTime frameDescription
Comfortthrough study completion, an average of 1monthChildbirth Comfort Questionnaire (CCQ); Each item ranks between 1 and 5 points: 1=Strongly disagree, 2=Mostly disagree, 3=Partially agree, 4=Mostly agree, and 5=Completely agree. Thus, the lowest and highest scores are 9 and 45 points, respectively. The higher the score one earns, the more comfortable they are; the lower the score, the exact opposite

Secondary

MeasureTime frameDescription
Labor painthrough study completion, an average of 1monthVisual Analog Scale (VAS); It is a 10-cm one-dimensional ruler; written on one end is no pain; on the other is worst pain. For the purpose of this study, the researchers used VAS vertically in this study, in line with the recommendations of other studies, who suggest that individuals understand VAS better when applied vertically.

Countries

Turkey (Türkiye)

Outcome results

None listed

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