Auricular Acupressure in Prehabilitation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorUniversity of Chicago

About this trial

Complementary medicine is recognized for its ability to enhance appetite, increase energy, reduce anxiety, decrease pain, and improve sleep, among many other benefits. Acupuncture is among the most frequent types of complementary medicine practiced in the US, and Medicare currently includes back pain as a reimbursable indication for this therapy. Acupuncture-related therapies may enhance efforts at prehabilitation in candidates for major lung resection.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being considered for major lung surgery

Surgery is not scheduled for at least 2 weeks

Age ≥ 50 years

Able to understand English at a 4th grade level

Disqualifiers

Allergy to Vaccaria seeds

Medical condition affecting either ear preventing use of auricular acupressure such as eczema, frostbite, sunburn

Trial design

Design model

Parallel

Treatments tested in this trial

  • Auricular Acupressure

    Other intervention

    Seeds will be placed during the clinic visit by the acupuncturist or the research associate according to the group the patient was assigned to. The care partner will observe the placement. A photograph of the seed placement will be taken and given to the care partner and to the patient after the relevant points are labeled by number or letter. The method of pressing is demonstrated for 1 one of the seeds, the care partner practices pressing on 2 other seeds, and the patient practices pressing on the remaining 2 seeds. Pressing consists of applying pressure, gradually increasing the pressure until the patient expresses discomfort, and maintaining that pressure until 2 minutes have passed. After pressing has been performed for each seed, the seeds are removed in clinic prior to clinic discharge.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Experimental GroupExperimental treatment 1 intervention
Group B: Control GroupSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Number of patients enrolled

The patient will complete a form after each seed pressing confirming the pressing and the time.

Time frame
2 weeks

Secondary outcomes

1

Ease of participation in the study.

The patient will complete a form after each seed pressing confirming the pressing and the time.

Time frame
End of Study (Week 4)

Other outcomes

1

Accuracy of seed placement by a non-professional care partner.

The care partner will place the seeds and then send a photo to the research team for correct seed placement verification or correction on a weekly basis. Accuracy of seed placement will be assessed by determining the number of corrections required to achieve seed placement each week.

Time frame
Weekly until Week 4
2

The change of the intervention prehabilitation results

Compared to the control group, the intervention will demonstrate better increases in endurance, function, mood, breathing capacity, and strength.

Time frame
End of Study (Week 4)

Sponsors and contacts

Click on the lead sponsor to view all of their trials.