Feasibility and Usability of EnergyPoints: A Mobile Health App to Guide Acupressure Use for Cancer Symptom Management.
Susan L Beck, Ryan Smith, Janet Mindes...
https://pubmed.ncbi.nlm.nih.gov/38284345/Actively Recruiting
Led by 5 Point App, Inc. · Updated on 2026-04-07
180
Participants Needed
1
Research Sites
13 weeks
Total Duration
Researchers are evaluating the EnergyPoints mobile phone app designed to guide cancer survivors in self-administering acupressure to reduce cancer-related fatigue and improve sleep. This decentralized clinical trial aims to validate the apps effectiveness on fatigue, sleep disturbances, and quality of life in a diverse group of adult cancer survivors both on and off treatment. The study addresses the need for accessible, non-pharmacologic symptom management options since fatigue and sleep issues affect many survivors and current therapies can be costly or hard to access. Participants will use the EnergyPoints app daily for six weeks to perform self-acupressure rituals, guided by the app on iOS or Android devices. The app offers customizable options for acupressure rituals and pressing durations and includes enhancements like aromatherapy, relaxing music, and social engagement features. The trial compares an Immediate Group that starts the app intervention right after a one-week baseline with a Wait-List Control Group that wears a Fitbit and completes surveys for six weeks before beginning the app use. The study collects data via Fitbit fitness trackers and daily and weekly self-reports. Participants join remotely and will wear a Fitbit continuously during the study, answering daily questions through the app and weekly surveys online. They will complete questionnaires and participate in an online interview at the end. The study measures fatigue, sleep quality, physical and mental health, step counts, and sleep efficiency over 7 or 13 weeks depending on group assignment. Safety monitoring includes minimal risks such as minor bruising from acupressure and privacy considerations related to app use. The total participation includes baseline, intervention, and follow-up periods with data collection throughout.
CONDITIONS
Decentralized Clinical Trial of Effectiveness of EnergyPoints App in Cancer Survivors
S
Susan L Beck, PhD
M
Melanie A Gold, DO
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5 Point App, Inc.
Lead Sponsor
National Cancer Institute (NCI)
Collaborating Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | EnergyPoints App | Wait-List Control |
|---|---|---|
| What it is | A mobile app guiding self-acupressure to address fatigue and sleep problems in cancer survivors, integrating daily rituals with symptom and sleep/activity tracking. | Participants assigned to wait-list control receive no app-based or other acupressure intervention during the trial and routine assessment only. |
| Role in trial | Test intervention group, randomized to receive guided self-acupressure and monitoring via the EnergyPoints app for 6 weeks. | Comparison group, randomized to receive no intervention during the study and monitored over the same period. |
| Primary use | For managing cancer-related fatigue and sleep disturbance, aiming to improve quality of life in cancer survivors. | Serves as a non-intervention comparator to measure outcomes relative to not receiving digital acupressure support. |
| How it is given or performed | Participants download the EnergyPoints mobile app (iOS or Android), which provides daily instructions to perform stimulating and relaxing acupressure rituals for 6 weeks along with integrated symptom self-reporting and wearable device data. | No intervention or digital app use; participants receive routine observation and outcome assessment only. |
| Evidence status | Prior feasibility studies found the app to be usable by cancer survivors, but effectiveness for reducing fatigue or sleep problems remains under investigation in this randomized trial. | Wait-list control does not provide active behavioral symptom management; no additional effect on fatigue or sleep is expected. |
| Important limitations | Requires daily engagement with a smartphone, basic sensory and functional capacity, and tolerance for wearable device use; the impact on long-term fatigue and sleep symptoms remains unproven. | Does not provide access to any fatigue, sleep, or quality of life intervention during the trial; participants may subsequently receive the app after the study period. |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (remote)
Duration - 6 weeks
Participants use the EnergyPoints app daily for 6 weeks to guide self-acupressure rituals for managing cancer-related fatigue and sleep disturbances. They can tailor rituals and use optional enhancements like aromatherapy, music, and visuals. Data on symptoms and activity are collected via the app and a Fitbit device.
Daily app use and continuous Fitbit monitoring; weekly self-report surveys
Duration - Up to 6 weeks
Participants continue to provide data through the app and Fitbit for an additional period after active app use to assess ongoing effects and usability.
Daily app use and Fitbit monitoring; weekly self-report surveys
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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Susan L Beck, Ryan Smith, Janet Mindes...
https://pubmed.ncbi.nlm.nih.gov/38284345/5 Point App, Inc.
Lead Sponsor
National Cancer Institute (NCI)
Collaborating Sponsor