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Pillars4Life Trial

Pillars4Life Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02465892
Acronym
Pillars4Life
Enrollment
284
Registered
2015-06-09
Start date
2015-05-31
Completion date
2016-10-31
Last updated
2017-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder Cancer, Breast Cancer, Cervical Cancer, Colon Cancer, Esophageal Cancer, Liver Cancer, Lung Cancer, Ovarian Cancer, Pancreatic Cancer, Prostate Cancer, Renal Cancer, Uterine Cancer

Keywords

cancer, stress, chronic pain, anxiety, coping, balance, online course, psychosocial, support, tools

Brief summary

This study aims to explore whether cancer patients can benefit from completing the Pillars4Life online coping program. This randomized control trial will have half its subject completing the program and the other half receiving standard care in order to measure whether the program is beneficial in dealing with stress, anxiety, and particularly chronic pain that often accompany a cancer diagnosis.

Detailed description

Subjects will complete three online surveys as part of the study. Each subject who completes the first survey will be randomized to either the control group who receive standard care from their care team or to complete the 9-week Pillars4Life curriculum. Subjects completing the Pillars4Life program will select a course day/time that works for them from those offered. Each week the program will send an email approximately 15 minutes before class time with a link. Subjects will click the link to go to the classroom, where they will enter their name and phone number. The program will call the number provided and the subject will listen to the audio over the phone, while watching the guide and activities in the virtual classroom on their computer. Each class will last about an hour. All subjects will complete two additional surveys, at approximately 9 weeks and 18 weeks after enrolling in the study.

Interventions

BEHAVIORALPillars4Life

The Pillars4Life program will guide participants through activities that will help to identify stress and anxiety triggers, plan ways to cope with the stress of life and cancer, manage anxiety, deal with chronic pain, and balance competing priorities in life.

Sponsors

Pfizer
CollaboratorINDUSTRY
Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Current pain level ≥3 and at least one prior score ≥3 on a 0-10 scale as reported in EPIC; * Age ≥18 years * Diagnosed with Breast, GI, GU, GYN, or Thoracic cancer * Actively receiving care at the Duke Cancer Center, Durham Regional Hospital, or Duke Raleigh Hospital * Able/willing to have an online interaction with the Pillars4Life online CORE program curriculum * Life expectancy ≥6 months * Providing informed consent * Able to read/write English.

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Chronic pain9 weeksSubjects will report how much chronic pain they have and how they are coping with it.

Secondary

MeasureTime frameDescription
Stress9 weeksSubjects will report how much stress they are under they have and how they are coping with it.
Anxiety9 weeksSubjects will report how much anxiety they have and how they are coping with it.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026