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Clinical Trials/NCT02409485
NCT02409485CompletedNot Applicable

Improving Self-Management in Head and Neck Cancer

Baylor College of Medicine2 sites in 1 country60 target enrollmentStarted: November 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
2
Primary Endpoint
Feasibility of the CST intervention as assessed by recruitment and retention rates

Study Overview

Brief Summary

By teaching skills to improve the coordination of care and support in couples coping with head and neck cancer (HNC), this couple-based psychosocial intervention holds great promise for improving self-management, reducing costly hospitalizations and treatment interruptions, and improving both partners' quality of life. Home-based delivery will enhance future dissemination and outreach to those who do not have access to psychosocial services or live far away from their care centers. If found effective, the intervention may also have salutary downstream effects on the health and well-being of HNC patients and their partners.

Detailed Description

Patients treated with radiation (XRT) for head and neck cancers (HNCs) experience significant side effects such as abnormally reduced salivation, difficulty swallowing, and taste changes even after they have been definitively treated. To control side effects and minimize discomfort, intensive self-care protocols are prescribed, but adherence is poor. Partners (spouses/significant others) can play a critical role in supporting adherence, but often lack knowledge, experience high rates of distress, and display poor communication (e.g., critical or controlling), that can interfere with patient self-care. The investigators have developed a home-based couples skills-training (CST) intervention that teaches: 1) self-management skills to control/prevent side-effects; 2) communication skills to facilitate coordination of care and support; and 3) strategies to improve communal coping and confidence in the ability to work as a team. The goal is to reduce healthcare utilization and improve multiple domains of patient and partner QOL. Specific aims are to: develop and evaluate the content and materials of the CST intervention (AIM 1) and evaluate its feasibility and acceptability (AIM 2). The multidisciplinary team will review and evaluate the content we have already developed based on the ongoing work with HNC couples (K07). Once content is finalized, tailored manuals will be developed for patients and partners and evaluated through two focus groups (AIM 1). The investigators expect that most couples (> 60%) approached will agree to participate and that CST will be well-accepted (AIM 2). Knowledge gained will be used to refine CST and to collect data on effect sizes and variation for a larger trial. Innovation: CST takes a multiple-behavioral approach to addressing and preventing HNC treatment side effects and, in the process, seeks to improve multiple domains of QOL. It is also the first program in HNC that actively involves both members of the couple to address barriers in the home environment in which self-management occurs. Finally, this study conceptualizes the couple relationship as a resource and leverages that resource to improve patient care and outcomes. Impact: Home-based delivery will enhance future dissemination and outreach to the target population. Overall, CST holds great promise for improving patient self-management behaviors, reducing costly hospitalizations and treatment interruptions, and improving multiple aspects of patient and partner QOL.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • patient is initiating radiotherapy for HNC
  • patient has Karnofsky score > 50 (ambulatory & capable of self-care)
  • patient lives with a partner (spouse/significant other - includes homo- and heterosexual couples)
  • patient/partner is able to provide informed consent
  • patient/partner is > age 18.

Exclusion Criteria

  • patient has significant comorbidities (e.g., HIV, transplant), or another illness that may require hospitalization
  • patient/partner cannot read or communicate using spoken English.
  • individuals with diminished mental capacity
  • prisoners
  • pregnant women

Outcomes

Primary Outcomes

Feasibility of the CST intervention as assessed by recruitment and retention rates

Time Frame: 6 months

recruitment and retention rates

Acceptability of the CST intervention as assessed by the program evaluation questionnaire

Time Frame: 6 months

satisfaction with the intervention by completing a program evaluation questionnaire developed by the study team that asks about perceived skills mastery and satisfaction with program content and logistics

Secondary Outcomes

  • Partners QOL measured by Short Form 12 (SF12)(6 months)
  • Short Form Dyadic Adjustment Scale (DAS7)(6 months)
  • PROMIS short form anxiety and depression(6 months)
  • Patient QOL measured by MD Anderson Symptom Inventory - Head and Neck (MDASI-HN)(6 months)
  • Healthcare utilization as assessed by number of hospitalizations and unplanned clinic visits(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hoda Badr

Associate Professor

Baylor College of Medicine

Study Sites (2)

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