30 Participants Needed

Acupressure for Cancer Survivors

Age: < 65
Sex: Any
Trial Phase: Academic
Sponsor: University of Michigan Rogel Cancer Center

Trial Summary

What is the purpose of this trial?

This clinical trial tests the feasibility of self-administered relaxing acupressure on fatigue in adolescent and young adult (AYA) cancer survivors. Acupressure, a type of complementary or alternative medicine, is the application of pressure or localized massage to specific sites on the body to control symptoms. Relaxing acupressure has been shown to improve cancer-related fatigue (CRF) in adults, however, less is known about the impact of relaxing acupressure on CRF in AYA cancer survivors."

Will I have to stop taking my current medications?

The trial does not specify if you need to stop your current medications, but you can continue usual treatments for fatigue if they started at least eight weeks before joining the study and the dose hasn't changed.

What data supports the effectiveness of the treatment Self-Administered Relaxing Acupressure for cancer survivors?

Research suggests that self-acupressure can help manage symptoms like pain, fatigue, and sleep issues in cancer patients undergoing chemotherapy. It has also been shown to significantly reduce fatigue in breast cancer survivors, making it a promising, easy-to-use, and non-toxic option for improving quality of life.12345

Is acupressure safe for cancer survivors?

Acupressure is generally considered safe for cancer survivors, with studies showing it to be non-toxic and easy to use. Very few minor side effects have been reported, and it has been used to manage symptoms like fatigue and nausea with positive outcomes.13456

How is the treatment Self-Administered Relaxing Acupressure unique for cancer survivors?

Self-Administered Relaxing Acupressure is unique because it is a non-toxic, easy-to-use treatment that cancer survivors can perform themselves to reduce symptoms like fatigue, pain, and insomnia, without the need for medication or in-person visits.12357

Research Team

RK

Robert Knoerl

Principal Investigator

University of Michigan Rogel Cancer Center

Eligibility Criteria

This trial is for adolescent and young adult cancer survivors who are experiencing fatigue. The specific eligibility criteria aren't provided, but typically participants must meet certain health conditions to be included.

Inclusion Criteria

I am between 15 and 39 years old.
Speak/read English
CRF started at or after the diagnosis of cancer
See 3 more

Exclusion Criteria

I am not starting new treatments for cancer-related fatigue during the study but can continue my current ones if they began 8 weeks before joining.
I have been diagnosed with anemia, a mood disorder, or hypothyroidism that hasn't been treated.
Plan to become pregnant or lactating during the study period
See 1 more

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants self-administer relaxing or sham acupressure using a mobile application and AcuWand for 27 minutes daily over 6 weeks

6 weeks

Follow-up

Participants are monitored for changes in fatigue and satisfaction with the intervention

4 weeks

Treatment Details

Interventions

  • Self-Administered Relaxing Acupressure
Trial Overview The study is testing if self-administered relaxing acupressure can reduce fatigue in these individuals. It involves using a medical device or technique to apply pressure on the body, along with questionnaires, interviews, and internet-based interventions.
Participant Groups
2Treatment groups
Experimental Treatment
Placebo Group
Group I: ARM I (relaxing acupressure)Experimental Treatment5 Interventions
Patients receive access to acupressure mobile application and an AcuWand on study and self-administer relaxing acupressure to 9 acupoints over 27 minutes QD for 6 weeks.
Group II: ARM II (sham acupressure)Placebo Group5 Interventions
Patients receive access to acupressure mobile application and an AcuWand and self-administer sham acupressure to non-acupressure point locations over 27 minutes QD for 6 weeks.

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Michigan Rogel Cancer Center

Lead Sponsor

Trials
303
Recruited
20,700+

Findings from Research

Self-acupressure was found to be feasible and showed clinical significance in reducing insomnia, anxiety, and depression symptoms in cancer patients, particularly in the true acupressure group after 4 weeks of intervention.
Both true and sham acupressure groups reported lower insomnia and anxiety scores compared to the enhanced standard care group, indicating potential effectiveness and a possible placebo effect in managing these symptoms.
Pilot randomized sham-controlled trial of self-acupressure to manage the symptom cluster of insomnia, depression, and anxiety in cancer patients undergoing chemotherapy.Hoang, HTX., Molassiotis, A., Chan, CW., et al.[2022]
A study involving 60 patients with pancreatic or colon cancer showed that self-acupressure significantly reduced pain, fatigue, and sleep disturbances compared to a control group that did not receive any intervention.
The intervention consisted of 16 self-acupressure sessions over 4 weeks, demonstrating that this method is an effective, accessible, and low-cost option for managing symptoms related to chemotherapy in cancer patients.
The Effects of Self-Acupressure on Pain, Fatigue, and Sleep Quality in Colon and Pancreatic Cancer Patients Receiving Chemotherapy: A Randomized Controlled Study.BahรงecioฤŸlu Turan, G., ร–zer, Z., YanmฤฑลŸ, S., et al.[2023]
A randomized clinical trial involving 375 breast cancer survivors is investigating the efficacy of two types of self-administered acupressure (relaxation and stimulating) in reducing moderate to severe fatigue, with assessments at baseline, 3 weeks, and 6 weeks.
Preliminary evidence suggests that acupressure could be a low-cost, non-toxic intervention that significantly alleviates cancer-related fatigue, potentially offering a practical self-care option for survivors.
Acupressure for persistent cancer-related fatigue in breast cancer survivors (AcuCrft): a study protocol for a randomized controlled trial.Zick, SM., Wyatt, GK., Murphy, SL., et al.[2022]

References

Pilot randomized sham-controlled trial of self-acupressure to manage the symptom cluster of insomnia, depression, and anxiety in cancer patients undergoing chemotherapy. [2022]
The Effects of Self-Acupressure on Pain, Fatigue, and Sleep Quality in Colon and Pancreatic Cancer Patients Receiving Chemotherapy: A Randomized Controlled Study. [2023]
Acupressure for persistent cancer-related fatigue in breast cancer survivors (AcuCrft): a study protocol for a randomized controlled trial. [2022]
Effect of self-acupressure for symptom management: a systematic review. [2022]
Virtual acupressure for symptom management in cancer populations during COVID-19: a retrospective analysis. [2023]
The efficacy of acupoint stimulation for the management of therapy-related adverse events in patients with breast cancer: a systematic review. [2022]
Relaxation acupressure reduces persistent cancer-related fatigue. [2022]
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