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Completed

NCT Number: NCT02069769

Ensuring Communication in Hospice by Oncology Study (ECHO)

The goal of this study is to determine if scheduled communication with the oncology team through phone calls is helpful to caregivers with the transition to hospice care.

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Key information

About this study

There are four parts of the study. First, the participant will receive phone calls twice a week from the oncology team to check in with how the transition to hospice is going. Second, the participant may choose to have an appointment with the Massachusetts General Hospital oncology team to discuss any questions or concerns regarding cancer care or the transition to hospice. Third, each week of hospice care, the participant will be asked to complete a set of questionnaires at a time that is convenient for them either by phone or by email. These questions will ask the participant about their recent thoughts and feelings about their experience with hospice and as a caregiver. The questions will take less than 15 minutes to answer. Fourth, after hospice care has ended, the participant will be called by the oncology team to again check in and about a month later, the participant will also be contacted by phone to complete a set of questionnaires, again asking about their thoughts and feelings about your experience with hospice and as a caregiver.

For all of the questionnaires, the participant may skip any questions that the participant prefers not to answer. The responses will remain confidential and will be available only to study staff members who are trained in confidentiality and research ethics.

Additionally, during the research study, the investigators will obtain information from the participant's loved one's Massachusetts General Hospital electronic medical record that is relevant to the participation in the study for up to 6 months. If he/she has visited another hospital during this time, the investigator will also ask the participant for their permission to obtain the medical records from this visit.

The participant will not receive any compensation for this study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult Patient Criteria

-->18years of age) with a diagnosis of an incurable malignancy of the head and neck, gynecological oncology, sarcoma, or melanoma

  • Receiving oncology care at the MGH Cancer Center
  • Referral to home hospice services in previous five business days.
  • Family Caregiver Eligibility Criteria:
  • Designated adult family/informal caregiver for an eligible patient who will provide the primary home care for the patient receiving hospice services
  • Ability to read and respond to questions in English or with the assistance of a translator
  • Access to telephone and/or computer to communicate with the oncology team and complete questionnaires
  • Willingness to complete weekly questionnaires via telephone or email.

Exclusion criteria

  • Patient Exclusion Criteria:

-- Referral to hospice services away from home (eg in nursing home or in an inpatient or residential setting)

  • Family Caregiver Exclusion Criteria --Person is not the primary caregiver for the patient

Treatment and study plan

communication with oncology team

Behavioral

Oncology team will contact patients and families via telephone at specific intervals

Primary outcomes

  1. Evaluate the feasibility of implementing the Ensuring Communication in Hospice by Oncology Study (ECHO) intervention by patients' family caregivers and their oncology providers.

    Time frame: 2 Years

    ECHO will be considered feasible if greater than 70% of participants have > 50% of the scheduled phone contact with the oncology team during hospice care, which will be documented in the patient's medical record. Feasibility will also be demonstrated if greater than 70% of the family caregivers completing the questionnaires do so greater than 50% of the time they were scheduled. Finally, feasibility will also be demonstrated if caregivers are able to be contacted and decide upon participation within 5 days of patient hospice enrollment.

Secondary outcomes

  1. Prospectively explore the satisfaction with the overall experience of family caregivers through questionnaires when receiving the ECHO intervention.

    Time frame: 2 Years

  2. Prospectively explore rates of health service utilization in the patients receiving the ECHO intervention in terms of (1) hospice disenrollment; (2) hospitalization; and (3) emergency department visits

    Time frame: 2 Years

  3. Prospectively explore the levels of stress of family caregivers through questionnaires when receiving the ECHO intervention.

    Time frame: 2 years

  4. Prospectively explore decision making regret of family caregivers through questionnaires when receiving the ECHO intervention.

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Registry information

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Feb 24, 2014
Registry last updated
Apr 18, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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