Decentralized Clinical Trial of Effectiveness of EnergyPoints App in Cancer Survivors

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
Sponsor5 Point App, Inc.

About this trial

The purpose of the study is to evaluate whether EnergyPoints, a mobile phone health app that guides the participant to do self-acupressure, can decrease fatigue and improve sleep. Acupressure consists of applying physical pressure with fingers or a device to small locations on the body called acupoints.

* The investigators will conduct this clinical trial remotely, allowing participants to use the app wherever they are. Participation will involve using the app daily while wearing a fitness tracker (a Fitbit) on the wrist, answering questions on the app and online, as well as completing a questionnaire and participating in an online interview at the end of the study. Participants will be assigned by chance to one of two groups. In both groups, participants will have a 1 week baseline week (Week 0) to get used to the Fitbit. Participants in the Immediate Group will start the 6 week trial of EnergyPoints immediately (Week 1). Participants in the Wait-List Group will be on a wait-list for 6 weeks during which time they will wear the Fitbit and answer online questions daily and weekly. At the end of the waiting period (week 7), these participants will begin the 6 week trial of EnergyPoints. * The risks to participating are minimal. There is a small risk of bruising or getting sore at a point where participants apply pressure. As with any mobile app, there is the possibility that electronic information could be viewed by third parties not involved in the study. The investigators cannot promise any benefits from participating in the study. However, it is possible that using acupressure might improve fatigue or sleep. Participants may use any other approaches to improve fatigue and sleep while in the study.

A pilot study will be conducted first with 8 participants and 1 week periods (1 week baseline, 1 week waitlist, and 1 week intervention followed by an End of Study Questionnaire and Exit Interview

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Have cancer or have been treated for cancer;

at least a moderate level of fatigue (greater than 4 on a 0 to 10 Likert-type scale);

able to read and speak in English;

age 18 years or older; Android 11 or later),

Disqualifiers

recent history of easy bruising or bleeding

previous use of the EnergyPoints app.

Trial design

Design model

Parallel

Treatments tested in this trial

  • App to guide self-acupressure

    Other intervention

    The intervention is delivered via a mobile health app. EnergyPoints app, on iOS and Android, educates and guides use of acupressure rituals to self-manage fatigue and sleep disturbances. The intervention involves using the app daily for 6 weeks. A follow-along format guides correct point stimulation for two acupressure rituals (stimulating and relaxing). The app synchronizes symptom self-reports with fitness tracker (e.g., an Apple Watch or Fitbit) sleep and activity data, allowing evaluation of response to acupressure. The dashboard provides options to tailor the rituals and pressing time (½, 1 or 2 min. per point) according to symptom experience, lifestyle, and schedule. Individuals can choose to use enhancements such as aromatherapy (including an instructional safety video), relaxing music, and/or visuals during each ritual and connect with other users via the social engagement feature.

Treatment groups

180 Participants
are divided into 2 treatment groups
Group A: Wait-List ControlNo intervention 0 interventions
Group B: App to guide self-acupressureExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Fatigue self-report 1

Patient-Reported Outcome Measurement Information System (PROMIS) Fatigue 7a, a standardized measure of fatigue, yields a T score. A T score is a standardized measure on a 0 to 100 scale. The mean is 50 and SD is 10. Higher results indicate more fatigue.

Time frame
Baseline and Weekly for 7 or 13 weeks
2

Fatigue self-report 2

Patient Reported Outcome Measurement Information System (PROMIS) single item of fatigue intensity on a 1 to 5 scale. A higher score indicates more fatigue.

Time frame
Daily for 7 or 13 weeks
3

Sleep Self-Report 1

Patient Reported Outcome Measurement Information System (PROMIS) Sleep Disturbances 8b, a standardized measure of sleep, yields a T score. A T score is a standardized measure on a 0 to 100 scale. The mean is 50 and SD is 10. Higher results indicate more sleep disturbance.

Time frame
Baseline and Weekly for 7 or 13 weeks
4

Sleep Self-Report 2

Single item measure of overall sleep quality on a scale of 1 to 5. A higher score indicates better sleep quality.

Time frame
Daily for 7 or 13 weeks

Secondary outcomes

1

Active Step Count

Fitbit is worn 24/7 and data are synched via the EnergyPoints app. Active minutes are calculated based on achieving a certain level of activity (with an algorithm). The measure in number of active minutes per 24 hours. The range is 0 to individual's maximum.

Time frame
Daily for 7 or 13 weeks
2

Number of Awakenings

The Fitbit is worn 24/7 to measure activity and sleep. The number of awakenings is the number of times the participants wakes up from sleep during a 24 hour period.

Time frame
Daily for 7 or 13 weeks
3

Total Sleep Time

The Fitbit is worn 24/7 to measure activity and sleep. Total sleep time is the total number of minutes that the participant sleeps in 24 hours.

Time frame
Daily for 7 or 13 weeks

Other outcomes

Sponsors and contacts

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

5 Point App, Inc.

Lead sponsor

National Cancer Institute (NCI)

Collaborator