ClinicalTrials.gg
CompletedNCT07409194Updated Oct 27, 2026

The Effect of Acupressure on Hyperbilirubinemia in Newborns: A Randomized Controlled Trial

An interventional study of Acupressure in Hyperbilirubinemia, sponsored by Yuzuncu Yil University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 38 Weeks to 42 Months. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Yuzuncu Yil University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled May 2025, registered Feb 2026).
Updated Oct 27, 2026Now CompletedStudy completion moved+1 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
38 Weeks to 42 Months
Sex
All
01

Study summary

This study is a randomized controlled trial conducted to evaluate the effect of acupressure application on hyperbilirubinemia in newborns. The study examined the effect of regular acupressure applications to specific points on serum bilirubin levels in newborns at risk of developing physiological jaundice in the first days of life. By comparing bilirubin levels between the experimental and control groups, the potential benefits of acupressure in reducing the severity of jaundice and supporting bilirubin metabolism were investigated. The findings suggest that acupressure can be used as a complementary method in neonatal care.

Read the detailed description

One of the most common problems encountered in the neonatal period is neonatal jaundice, which develops due to an increase in indirect bilirubin (Özdemir and Yılmaz, 2019). Jaundice (hyperbilirubinemia) is defined as the yellowing of the skin and the whites of the eyes due to the accumulation of bilirubin in the skin and mucous membranes of newborns (Kılıç and Yılmaz, 2021). Jaundice is a common condition seen in 60% of term infants and more than 80% of preterm infants (Muniyappa and Kelley, 2020). Hyperbilirubinemia (HB), which is frequently seen in newborns, especially in the indirect form, is a mild health problem in most cases (Olcar, 2019; Yılmaz, 2019). HB in newborns usually progresses cephalocaudally (from head to toe); it starts in the face and spreads to the body as serum bilirubin levels increase (Turkish Neonatology Association [TND], 2022). Symptoms such as lethargy and feeding difficulties may occur in infants with severe HB. If not treated promptly, serious neurological complications such as kernicterus may occur. Early diagnosis, close monitoring, and treatment are vital to prevent potential damage in newborns (Muniyappa and Kelley, 2020).

Various treatment methods have been developed to reduce bilirubin levels. Among these methods, the most commonly used are blood exchange, phototherapy, and drug treatments (Garg et al., 2019; Kılıç and Yılmaz, 2021). To support neonatal HB treatment, studies evaluating the effectiveness of non-pharmacological and complementary applications, in addition to pharmacological methods, have also been conducted (Öztürk, 2025; Coşkun and Karakoç., 2025; Wu et al., 2022).

Acupressure is a complementary treatment method that aims to control symptoms by applying pressure to specific points on the meridians (İskender and Çalışkan, 2020). During the application, sensitive pressure is applied to specific points on the body using the hands and fingers, and in some cases, special tools; this aims to regulate energy flow and support the body's natural healing processes (Dincer et al., 2022; Harris et al., 2020). These stimuli, applied through touch, can activate receptors in the skin of infants with HB and be transmitted to the brain centers via reflex pathways. This can stimulate the parasympathetic nervous system and the vagus nerve, accelerating bowel movements, contributing to the regulation of the digestive system, and helping to expel meconium more quickly (Roth and Sullivan, 2006). In this regard, it is crucial to correctly identify the appropriate acupressure points during the treatment process (Bayraktar, 2023).

The application of acupressure has been used in various clinical settings in the neonatal and pediatric populations, and its effects on different physiological outcomes have been investigated. The effects of acupressure on pain (Altıntaş, 2023; Oğul, 2023; Özkan and Balcı, 2018), infantile colic (Özgören, 2021), and chemotherapy-induced nausea and vomiting (Balcı, 2018) in the pediatric group have been examined in various studies. However, it has been determined that studies evaluating the effect of acupressure on HB in newborns (Wu et al., 2022) are quite limited. Therefore, the aim of this study is to evaluate the effect of acupressure applied to newborns on HB. In this context, the potential contributions of acupressure to reducing serum bilirubin levels and supporting the treatment process will be examined, and it is aimed that the findings will provide scientific evidence regarding the effectiveness of acupressure as a complementary approach in the management of hyperbilirubinemia and guide clinical practice.

02

Conditions studied

  • Hyperbilirubinemia

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03

In context

Hyperbilirubinemia

81 studies on the registry are indexed under Hyperbilirubinemia; 11 are open to participants now.

This study's enrollment of 60 is below the median of 81 across 50 interventional studies indexed under Hyperbilirubinemia.

Browse Hyperbilirubinemia studies →

Lead sponsor

Yuzuncu Yil University is the lead sponsor of 78 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
38 Weeks to 42 Months
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Gestational age ≥38 weeks
  • Diagnosed with neonatal hyperbilirubinemia
  • Hospitalized in the neonatal unit for at least 24 hours
  • Birth weight ≥2500 g
  • Written obtained from parents

Exclusion criteria

Exclusion Criteria:

  • Preterm newborns
  • Congenital metabolic disease or congenital anomalies
  • Hemodynamically unstable newborns
  • Newborns whose parents did not provide consent
  • Newborns with any condition preventing acupressure application
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Single (Participant)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Acupressure Group

    Newborns assigned to the intervention group receive standard acupressure at predetermined acupuncture points (ST36 - Zusanli and KI1 - Yongquan) by a trained practitioner 0 and 12 hours after birth. Each session lasts approximately 4 minutes. Total serum bilirubin levels are measured 24 hours after birth. All newborns continue to receive routine newborn care and feeding according to the unit protocol.

    Behavioral: Acupressure

  • No intervention
    Control Group

    Newborns assigned to the control group receive routine neonatal care and feeding according to unit protocol without any acupressure intervention. Total serum bilirubin levels are measured at the 24th hour of life.

Interventions

  • BehavioralAcupressure

    Acupressure intervention

06

What researchers measure

Primary outcomes

  1. Total Serum Bilirubin Level

    Measurement of total serum bilirubin level to evaluate the effect of acupressure on neonatal hyperbilirubinemia.

    Time frame: 24 hours after birth

07

Study locations

1 site
  • Van Yuzuncu Yil University
    Van, 65100, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from May 2025 to primary completion in Feb 2026, 9 months.

Of 22 interventional studies with no phase under Hyperbilirubinemia, half reached primary completion within 9 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 19. This study's 9 months is close to that.

Completion moved once since we started tracking on Sep 25, 2026: Aug 2026 → May 2026, on Oct 27, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Feb 6, 2026
First posted
Feb 13, 2026
StartActual
May 5, 2025
Primary completionActual
Feb 5, 2026
CompletionActual
May 15, 2026was Aug 2026
Last update
Oct 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Enrolling by invitation→Completed
changed Oct 27, 2026
Study completion
Aug 5, 2026→May 15, 2026 (actual)
Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    Enrolling by invitation→Completed
    Study completion Aug 5, 2026→May 15, 2026 (now actual)
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07409194
Lead sponsor
Yuzuncu Yil University
Responsible party
Veysel Can (MD, PhD, Yuzuncu Yil University) — Principal investigator
First posted
Feb 13, 2026
Start date
May 5, 2025
Primary completion
Feb 5, 2026
Completion
May 15, 2026
Last update
Oct 27, 2026

Study contacts

Veysel CAN, MD, PhD
principal investigator · Yuzuncu Yil University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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