CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 42 enrolled / 42 target
Drug / intervention
Acupressure Therapy +4 moreprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06442891
NCT06442891N/ACompletedHigh Momentum (2.0/mo)Completion was 6mo ago
CompareCT.gov

A Pilot Study of Self-Administered Acupressure for Fatigue Among Adolescent and Young Adult (AYA) Cancer Survivors

University of Michigan Rogel Cancer Center·interventional·Posted Jun 4, 2024·Updated Jun 23, 2026

In Brief

A clinical study evaluating Acupressure Therapy, Internet-Based Intervention, and 2 other interventions for Hematopoietic and Lymphatic System Neoplasm and Malignant Solid Neoplasm. Completed, enrolled 42 participants across 1 site.

Signals

Enrolling ahead of pace

Detailed Summary

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."

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHematopoietic and Lymphatic System Neoplasm, Malignant Solid Neoplasm
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20252026
First PostedJun 4, 2024
Enrollment StartOct 1, 2024
Primary CompletionDec 22, 2025
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 2.1 years ago

Arms & Interventions

ARM I (relaxing acupressure)experimental

Patients receive access to acupressure mobile application and self-administer relaxing acupressure to 9 acupoints over 27 minutes QD for 6 weeks.

Procedure: Acupressure TherapyOther: Internet-Based InterventionOther: InterviewOther: Questionnaire Administration
ARM II (sham acupressure)placebo_comparator

Patients receive access to acupressure mobile application and self-administer sham acupressure to non-acupressure point locations over 27 minutes QD for 6 weeks.

Procedure: Acupressure TherapyOther: Internet-Based InterventionOther: InterviewOther: Questionnaire Administration

Interventions

Acupressure Therapyprocedure

Self-administer relaxing acupressure

Acupressure Therapyprocedure

Self-administer sham acupressure

Internet-Based Interventionother

Receive access to acupressure mobile app

Interviewother

Ancillary studies

Questionnaire Administrationother

Ancillary studies