A Tailored, Web-based Program (COMPASS) to Improve Exercise and Dietary Changes in Stage I-III Pancreatic Cancer Patients Receiving Neoadjuvant Chemotherapy

Официальное название

Community for Physical Activity and Supportive Nutrition Strategies (COMPASS)

Обзор

This clinical trial studies whether a tailored, web-based program (web portal), Community for Physical Activity and Supportive Nutrition Strategies (COMPASS), can be used to improve exercise and dietary changes in patients with stage I-III pancreatic cancer who are receiving chemotherapy before surgery (neoadjuvant). Pancreatic cancer is a rare and understudied cancer, particularly in the area of promoting a healthy lifestyle to preserve physical and mental well-being during a long and difficult treatment regimen. Since pancreatic cancer is rare, programs have limited resources available to reach the patients who could benefit from programs aimed at promoting exercise and a healthy diet. The COMPASS web-portal is easily accessed by the patient via a computer, tablet, or phone. It is tailored to the unique needs of pancreatic cancer patients and provides exercise and diet recommendations along with behavioral support as they undergo the long process of cancer therapy. This may be a more effective way to reach and engage with the patient, which may improve exercise and dietary changes in stage I-III pancreatic cancer patients receiving neoadjuvant chemotherapy.

Подробное описание

PRIMARY OBJECTIVE:

I. Acceptability of the COMPASS web portal will be assessed through accrual, study retention, end-of-study focus groups, and exit surveys, while feasibility will be measured by adherence to prescribed recommendations, frequency of portal visits, and aggregate web portal usage data.

SECONDARY OBJECTIVE:

I. To evaluate the preliminary effectiveness of COMPASS on exercise and diet habits, self-efficacy for behavior change, stages of change for exercise, changes in physical and mental well-being, and treatment tolerance (treatment-related symptoms, side effects, # of dose reductions) at baseline, 3 months and post chemotherapy.

TERTIARY OBJECTIVE:

I. To compare outcomes between participants assigned to a single health coaching session or monthly coaching sessions.

OUTLINE: Patients are randomized to 1 of 2 groups.

GROUP 1: Patients receive access to COMPASS portal, a tailored exercise intervention which may consist of strength, aerobic, balance, and flexibility exercises, and tailored diet recommendations for the duration of neoadjuvant chemotherapy. Patients also attend two review sessions to discuss the tailored exercise intervention and dietary recommendations and may optionally receive motivational and support text messages three times a week (TIW) on study.

GROUP 2: Patients receive access to COMPASS portal, a tailored exercise intervention which may consist of strength, aerobic, balance, and flexibility exercises, and tailored diet recommendations for the duration of neoadjuvant chemotherapy. Patients also attend two review sessions to discuss the tailored exercise intervention and dietary recommendations and receive a coaching call once a month on study. Additionally, patients may optionally receive motivational and support text messages TIW on study.

Вмешательства

• Поведенческое Physical Activity and Nutritional Recommendations and Support
  Web-based lifestyle program that provides tailored nutrition and physical activity recommendations and web-based support strategies including text messages, electronic trackers, and coaching

Первичные конечные точки

• Accrual (Acceptability) [Срок оценки: Up to 12 months]
• Study retention (Acceptability) [Срок оценки: Up to 12 months]
• Listening session [Срок оценки: At completion of neoadjuvant chemotherapy (average of 6 months)]
• Exit survey [Срок оценки: At completion of neoadjuvant chemotherapy (average of 6 months)]
• Study intervention adherence (Feasibility) [Срок оценки: Up to 12 months]
• Web portal visit frequency (Feasibility) [Срок оценки: Up to 12 months]
• Web portal aggregate activity (Feasibility) [Срок оценки: Up to 12 months]

Вторичные конечные точки (12)

• Change in self-report physical activity behavior [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in dietary behavior [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in objectively measured physical activity (kcal/week) [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in objectively measured physical activity (daily step count) [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in Self-efficacy for Exercise score [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in stages of change for exercise [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Healthy Eating and Weight Self-Efficacy [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in self-report physical functioning, quality of life, and cancer related symptoms [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Symptom Measures [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in cognitive function [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in neuropathy [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]
• Change in pain [Срок оценки: At baseline, 3 months, and the completion of neoadjuvant chemotherapy up to 12 months]

Критерии участия

Критерии включения

• Age 18 years or older on date of enrollment

• Confirmed by review of the date of birth as documented in the electronic medical record (EMR) and subsequently recorded in a case report form (CRF)
• Diagnosed with stage I-III pancreatic cancer

• Confirmed by EMR review. In cases where the EMR is unclear, their physician will be contacted and asked to confirm
• Scheduled to receive neoadjuvant chemotherapy at Oregon Health \& Science University (OHSU)

• Confirmed by EMR review. In cases where the EMR is unclear, their physician will be contacted and asked to confirm
• Willing to adhere to the study protocol

• Confirmed verbally with the participant and response documented in the Participant Tracking database

Критерии исключения

• Cognitive difficulties that preclude answering the survey questions, participating in the intervention, or giving informed consent

• In the event of a suspected undeclared cognitive impairment, it will be confirmed by physician clearance or professional opinion of the Principal Investigators, Dr. Kerri Winters-Stone and/or Dr. Jackilen Shannon
• A medical condition, movement or neurological disorder, or medication use that contraindicates participation in light intensity exercise

• Confirmed by a combination of reviewing the EMR, and self-report during the initial screening call. If in the professional opinion of the Principal Investigator, Dr. Kerri Winters-Stone or Dr. Jackilen Shannon, contraindications other than those identified by the patient or physician are present, she may consider the participant ineligible
• Not fluent in English and therefore incapable of answer survey questions, reading the intervention web portal, and providing informed consent in English

• Confirmed verbally with the participant and response documented in the Participant Tracking database

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Поддерживающая терапия

Центры проведения

США · 1 центр

• OHSU Knight Cancer Institute — Portland

Идентификаторы

NCT: NCT07651358 · STUDY00028600

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗