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Completed

NCT Number: NCT02409485

Improving Self-Management in Head and Neck Cancer

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Baylor College of Medicine

Houston, Texas, 77030, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Couples Skill-Training (CST)

Behavioral

Patients and partners each receive a workbook and 6 one-hour telephone sessions with a Masters level trained interventionist. Manual content is tailored based on role (patient or partner). Couples participate together via speaker phone for half the sessions and patients and partners receive separate (individual) intervention calls for the other half of the sessions.

Primary outcomes

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

    Time frame: 6 months

    recruitment and retention rates

  2. 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

  1. PROMIS short form anxiety and depression

    Time frame: 6 months

    measures distress with Patient Reported Outcomes Measurement Information System (PROMIS) short form for anxiety and depression

  2. Patient QOL measured by MD Anderson Symptom Inventory - Head and Neck (MDASI-HN)

    Time frame: 6 months

    measures QOL for patients

  3. Partners QOL measured by Short Form 12 (SF12)

    Time frame: 6 months

    measures QOL for partners

  4. Short Form Dyadic Adjustment Scale (DAS7)

    Time frame: 6 months

    measures Relationship functioning

  5. Healthcare utilization as assessed by number of hospitalizations and unplanned clinic visits

    Time frame: 6 months

    number of hospitalizations and unplanned clinic visits

Sponsors and collaborators

Lead sponsor

Baylor College of Medicine

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Important dates

Study start
2014
Primary completion
2018
Study completion
2019
First posted
Apr 6, 2015
Registry last updated
Jan 18, 2020

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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