Head and Neck Cancer, Nutrition Aspect of Cancer, Survivorship
Conditions
Keywords
mHealth, Head and Neck Cancer, Survivorship, Caregiver
Brief summary
Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be enrolled to pilot test a nutrition support system with a care planning clinic visit and a caregiver mobile App. Participants will be asked to complete baseline and 6-week follow-up surveys. The clinic session (offered in person or remotely) will include a needs assessment and a tailored care plan with information, educational materials and referrals about participants' symptoms, behaviors, social concerns and caregiving tasks. After the visit, the program will provide an App for caregivers with follow-up resources and mobile support for one month.
Detailed description
The long-term goal of this research is to improve physical, emotional and social post-treatment outcomes in head and neck cancer survivors and caregivers by implementing a nutrition-focused mobile-Support program to prepare and support caregivers after treatment. Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be recruited to a single-arm intervention study to evaluate the feasibility, acceptability and short-term effects of a nutrition-focused mobile support system. The intervention includes 1) a clinic visit (offered in-person or virtually) with a tablet-based needs assessment at the end of or after completing treatment which will generate 2) a tailored care plan with messages, educational materials and referrals mapped to survivor and caregiver-endorsed concerns and 3) a caregiver App with encouragement, reminders and tips delivered through messaging and peer videos. Participants will complete baseline and 6-week follow-up surveys.
Interventions
The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support.
Sponsors
Study design
Eligibility
Inclusion criteria
Patient Inclusion Criteria: * 18 years and older * Patients with stage I-IVB HNC of the upper aerodigestive tract (including lip/oral cavity, nasopharynx, salivary gland, oropharynx, hypopharynx, paranasal sinus, and larynx cancers and cutaneous cancers of the head and neck region) * In the last two weeks of treatment to 3 months following completion of primary treatment (i.e., any combination of surgery, chemotherapy and radiation therapy) within the past 3 months * Experienced nutritional challenges at the end of treatment as assessed in a 6-item screener Patient
Exclusion criteria
* head and neck cancer patients who do not undergo treatment * Patients who do not read or understand English * Patients who are cognitively impaired and cannot complete interviews, as judged by the referring health care provider * Patients who do not have a smartphone for use in the study Caregiver Inclusion Criteria: * 18 years and older * Provide care for a loved one with stage I-IVB head and neck cancer who has completed treatment Caregiver
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | 6 week follow-up visit | Investigator developed questionnaire investigating acceptability of session intervention and care plan. Items were rated on a 6-point descriptive scale from strongly disagree to strongly agree. Participants that meet criteria are those that chose moderately or strongly agree. Items included: Session made me feel prepared, care plan information was helpful emotionally, care plan was helpful practically, amount of information in care plan provided was appropriate, timing of session of session was appropriate. |
| Intervention Delivery/ Fidelity | 6 week follow up visit | Number of caregivers receiving all session content and delivery of the intervention as planned (intro to session, nurse care plan discussion, viewed nutritional support video, app training). |
| Intervention Reach | Baseline and 6 week follow up visit | Percentage of those recruited who completed baseline and 6 week follow up surveys and the intervention session. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| PROMIS Depression- Short Form (SF) v1.0 Form 8A | Baseline and 6 week follow-up visit | PROMIS Depression- SF v1.0 form 8A is an 8-item Patient-Reported Outcomes Measure Information System (PROMIS) short-form instrument. Respondents are asked how often in the past 7 days they have experienced specific depression symptoms, using a 5-point ordinal rating scale of Never, Rarely, Sometimes, Often, and Always whereby a higher score indicates higher depression. Raw score totals are converted to an item response theory-based T-scores. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10 with a range of 38.2 to 81.3. Therefore, a person with a T-score of 40 is one SD below the mean. A decrease in change from baseline to 6 week followup indicates reduced depression. |
| Mean Score of Survivorship Readiness/Caregiver Preparedness | Baseline and 6 week follow-up visit | The 11-item Preparing for Life As a New Survivor (PLANS) Knowledge Subscale, developed at the University of Michigan, is utilized to evaluate survivor and caregiver (1) knowledge of diagnosis, treatment and side effects, and (2) communication with the cancer team regarding diagnosis, treatment and side effects and 3) preparedness for what to expect over the next year. Items are rated on a 6-point scale where: strongly disagree=1, moderately disagree =2, slightly disagree=3, slightly agree= 4, moderately agree=5 and strongly agree=6. Items were averaged, with a range of 1-6 with higher scores indicating higher levels of agreement. |
| Mean Score of Self-Efficacy | Baseline and 6 week follow-up visit | Based on the National Cancer Institute Follow-up Care Use Among Survivors (FOCUS) survey, two questions were asked: How confident are you that you can get advice or information related to your/your loved one's cancer if you needed at this time? and How confident are you that you can (assist your loved one to) keep to the follow-up care schedule recommended by your doctors? Participants rated items on a 5-point Likert scale where 0=Not at all confident to 4= Completely confident. Scores were averaged for each question, whereby higher scores indicated higher level of confidence. Change from baseline to 6 week follow up is also reported. Negative change indicates decline in self-efficacy. |
| Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Baseline and 6 week follow-up visit | PROMIS Scale v1.2 - Global Health short form consists of 10 items that assess overall perceived quality of life and five general domains of health and functioning including overall physical health, mental health, social health, pain, and fatigue. Scoring uses a 5-point Likert scale with the response scores reversed (5=None to 1=Very severe) so that higher scores for responses always indicate better health. Raw scores are summed and converted to a T-score (mean score of 50, SD ± 10), Therefore a person with a T-score of 40 is one SD below the mean. A decrease in the change from baseline to 6 week follow up indicates worsening quality of life, whereas an increase indicates improvement. |
| Caregiver Burden | Baseline and 6 week follow up visit | 4-item screening version of the Zarit Burden Interview is a self-report measure of caregiver burden. Caregivers rate each item on a 5-point Likert scale (0=never, 4= nearly always). Higher scores indicate greater caregiver distress. Total score range: 0 to 16, ≥ 8: high burden. An increase in change from baseline to 6 week follow up visit indicates increased caregiver distress. |
| Ease of Mobile App Use/User Engagement | 4 weeks during app use | Number of weekly prompt responses missed out of 184 total expected (23 caregivers given 2 prompts per week for 4 weeks). |
| Mean Score of Dyadic Coping/ Dyadic Efficacy | Baseline and 6 week follow-up visit | Dyadic Coping was measured using a 5-item cancer-specific subscale version of the Dyadic Coping Inventory. Items are rated on a 5-point scale from 1 (never) to 5 (always). Scores were averaged with a higher score indicating a better outcome. A decrease in change between baseline and 6 week followup visit indicates worsening outcome over time. Dyadic Efficacy is an investigator developed 1-item question How confident are you that you and your loved one can work together as a team to manage the cancer-related problems that come up? Item was answered on a scale of 0 (not at all confident) to 10 (extremely confident), with average score reported. A decrease in change between baseline and 6 week followup visit indicates worsening, where as an increase in change indicates improvement. |
| Percentage of Participants Rating App Satisfaction/ Perceived Importance | 6 week follow up visit | Ratings of satisfaction with app and prompts on a 6 point descriptive rating scale ranging from strongly agree to strongly disagree. Measurements reported below are count of participants who moderately or strongly agreed with individual prompts. |
| Process Monitoring Data | After session completion | Resources needed: Session length overall, length of nursing portion of session, length of app training- number of minutes |
| Change From Baseline in Nutritional Status Scale | Baseline and 6 week follow up visit | Investigator-developed 1 item: During the past two weeks, how satisfied have you been with your nutritional status (from Extremely satisfied (1) to Not at all satisfied (5))? |
| Change From Baseline in Symptom Distress/Symptom Management | Baseline and 6 week follow up visit | Adapted Symptom Distress Scale 1 item scaled to assess how distressing symptoms are to participant. 0= not at all distressing, 10= extremely distressing 1 item to assess patient and caregiver perceptions concerning patient ability to manage symptoms. 0= can manage extremely well, 10= cannot manage at all |
| Change From Baseline in Emotional Support | Baseline and 6 week follow up visit | PROMIS Short Form v2.0 - Emotional Support - 4a is a 4-item questionnaire. Item banks (currently adults only) assess perceived feelings of being cared for and valued as a person; having confidant relationships. PROMIS instruments are scored using item-level calibrations. Each question usually has five response options ranging in value from one to five. Raw scores are the sum of values of the response to each question then rescaled to to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10. Therefore a person with a T-score of 40 is one SD below the mean. |
| Change From Baseline in Symptom Severity | Baseline and 6 week follow up visit | MD Anderson Symptom Inventory (MDASI) Head and Neck Module- Includes 13 core items and an additional 9 head and neck cancer module items which calculates a total score of symptom severity. The MDASI assesses the severity of symptoms at their worst in the last 24 hours on a 0-10 Numeric Rating Scale, with 0 being not present and 10 being as bad as you can imagine. Core items and module symptom items are averaged into a mean module severity. A higher score always indicates an increase in severity. A decrease in change from baseline to 6 week follow up indicates improvement of symptoms. |
| Number of Participants With Care Plan Use Endpoints | 6 week follow up visit | Number of participants of use of care plan after session, including patient and caregiver report of Referred to Care Plan again, Used Care Plan, Used educational materials, and Shared Care Plan with others. |
| Ease of Use/System Usability | 6 week follow up visit only (no baseline comparison) | System Usability Scale (SUS) - The SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Scores range from 0-100, with higher scores indicating better usability. |
| Mean Score of Unmet Needs | Baseline and 6 week follow up visit | 30-item Cancer Survivors/Partners Unmet Needs instruments (CaSUN/ CaSPUN). Needs were endorsed on a yes/no basis, with a range of 0-30 total endorsed needs. A higher score indicates more endorsed needs. Average number of needs is reported. |
Countries
United States
Participant flow
Recruitment details
Head and neck cancer patients and caregivers were recruited at the end of radiation therapy.
Participants by arm
| Arm | Count |
|---|---|
| HEART Patients and caregivers will complete a HEART visit virtually or in person. The visit includes a needs assessment that generates a tailored care plan with messages, referrals and educational materials for discussion with a nurse. Caregivers will receive brief training about the HEART App and then use the App for 4 weeks with bi-weekly real-time prompts and feedback.
Heart APP: The HEART intervention includes a care planning visit for patients and caregivers and an App for caregivers focused on nutrition, self-care and support. | 46 |
| Total | 46 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | Lost to Follow-up | 4 |
Baseline characteristics
| Characteristic | HEART |
|---|---|
| Age, Continuous Caregivers | 59 years |
| Age, Continuous Patients | 63 years |
| Ethnicity (NIH/OMB) Caregiver Hispanic or Latino | 0 Participants |
| Ethnicity (NIH/OMB) Caregiver Not Hispanic or Latino | 23 Participants |
| Ethnicity (NIH/OMB) Caregiver Unknown or Not Reported | 0 Participants |
| Ethnicity (NIH/OMB) Patient Hispanic or Latino | 0 Participants |
| Ethnicity (NIH/OMB) Patient Not Hispanic or Latino | 23 Participants |
| Ethnicity (NIH/OMB) Patient Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) Caregivers American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Caregivers Asian | 0 Participants |
| Race (NIH/OMB) Caregivers Black or African American | 3 Participants |
| Race (NIH/OMB) Caregivers More than one race | 0 Participants |
| Race (NIH/OMB) Caregivers Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Caregivers Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) Caregivers White | 20 Participants |
| Race (NIH/OMB) Patients American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Patients Asian | 0 Participants |
| Race (NIH/OMB) Patients Black or African American | 4 Participants |
| Race (NIH/OMB) Patients More than one race | 0 Participants |
| Race (NIH/OMB) Patients Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Patients Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) Patients White | 19 Participants |
| Region of Enrollment United States | 46 participants |
| Sex: Female, Male Caregivers Female | 18 Participants |
| Sex: Female, Male Caregivers Male | 5 Participants |
| Sex: Female, Male Patients Female | 7 Participants |
| Sex: Female, Male Patients Male | 16 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 23 | 0 / 23 |
| other Total, other adverse events | 0 / 23 | 0 / 23 |
| serious Total, serious adverse events | 0 / 23 | 0 / 23 |
Outcome results
Intervention Delivery/ Fidelity
Number of caregivers receiving all session content and delivery of the intervention as planned (intro to session, nurse care plan discussion, viewed nutritional support video, app training).
Time frame: 6 week follow up visit
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| HEART Patients | Intervention Delivery/ Fidelity | 19 Participants |
Intervention Reach
Percentage of those recruited who completed baseline and 6 week follow up surveys and the intervention session.
Time frame: Baseline and 6 week follow up visit
Population: 50 enrolled, 4 lost to follow up
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| HEART Patients | Intervention Reach | 46 Participants |
Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria
Investigator developed questionnaire investigating acceptability of session intervention and care plan. Items were rated on a 6-point descriptive scale from strongly disagree to strongly agree. Participants that meet criteria are those that chose moderately or strongly agree. Items included: Session made me feel prepared, care plan information was helpful emotionally, care plan was helpful practically, amount of information in care plan provided was appropriate, timing of session of session was appropriate.
Time frame: 6 week follow-up visit
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| HEART Patients | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Care plan information was helpful emotionally | 17 participants |
| HEART Patients | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Amount of information in the care plan provided was appropriate | 18 participants |
| HEART Patients | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Care plan was helpful practically | 18 participants |
| HEART Patients | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Session timing was appropriate | 13 participants |
| HEART Patients | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Session made me feel prepared | 18 participants |
| HEART Caregivers | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Session timing was appropriate | 9 participants |
| HEART Caregivers | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Session made me feel prepared | 18 participants |
| HEART Caregivers | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Care plan information was helpful emotionally | 15 participants |
| HEART Caregivers | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Care plan was helpful practically | 18 participants |
| HEART Caregivers | Number of Participants Meeting Patient-Caregiver Session and Care Plan Acceptability Criteria | Amount of information in the care plan provided was appropriate | 20 participants |
Caregiver Burden
4-item screening version of the Zarit Burden Interview is a self-report measure of caregiver burden. Caregivers rate each item on a 5-point Likert scale (0=never, 4= nearly always). Higher scores indicate greater caregiver distress. Total score range: 0 to 16, ≥ 8: high burden. An increase in change from baseline to 6 week follow up visit indicates increased caregiver distress.
Time frame: Baseline and 6 week follow up visit
Population: Change in mean score from baseline to six weeks measured in caregivers only
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Caregiver Burden | Baseline | 1.8 units on a scale |
| HEART Patients | Caregiver Burden | 6 Week follow up visit | 1.9 units on a scale |
| HEART Patients | Caregiver Burden | Change from baseline to 6 week follow up visit | 0.1 units on a scale |
Change From Baseline in Emotional Support
PROMIS Short Form v2.0 - Emotional Support - 4a is a 4-item questionnaire. Item banks (currently adults only) assess perceived feelings of being cared for and valued as a person; having confidant relationships. PROMIS instruments are scored using item-level calibrations. Each question usually has five response options ranging in value from one to five. Raw scores are the sum of values of the response to each question then rescaled to to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10. Therefore a person with a T-score of 40 is one SD below the mean.
Time frame: Baseline and 6 week follow up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Change From Baseline in Emotional Support | Baseline | 56.0 T-Score |
| HEART Patients | Change From Baseline in Emotional Support | 6 week follow up visit | 55.7 T-Score |
| HEART Patients | Change From Baseline in Emotional Support | Change from baseline to 6 week follow up visit | -0.3 T-Score |
| HEART Caregivers | Change From Baseline in Emotional Support | Baseline | 52.0 T-Score |
| HEART Caregivers | Change From Baseline in Emotional Support | 6 week follow up visit | 52.8 T-Score |
| HEART Caregivers | Change From Baseline in Emotional Support | Change from baseline to 6 week follow up visit | 0.8 T-Score |
Change From Baseline in Nutritional Status Scale
Investigator-developed 1 item: During the past two weeks, how satisfied have you been with your nutritional status (from Extremely satisfied (1) to Not at all satisfied (5))?
Time frame: Baseline and 6 week follow up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Change From Baseline in Nutritional Status Scale | Change from baseline to 6 week follow up visit | -0.5 score on a scale |
| HEART Patients | Change From Baseline in Nutritional Status Scale | Baseline | 3.5 score on a scale |
| HEART Patients | Change From Baseline in Nutritional Status Scale | 6 week follow up visit | 3.0 score on a scale |
| HEART Caregivers | Change From Baseline in Nutritional Status Scale | 6 week follow up visit | 2.5 score on a scale |
| HEART Caregivers | Change From Baseline in Nutritional Status Scale | Baseline | 3.3 score on a scale |
| HEART Caregivers | Change From Baseline in Nutritional Status Scale | Change from baseline to 6 week follow up visit | -0.8 score on a scale |
Change From Baseline in Symptom Distress/Symptom Management
Adapted Symptom Distress Scale 1 item scaled to assess how distressing symptoms are to participant. 0= not at all distressing, 10= extremely distressing 1 item to assess patient and caregiver perceptions concerning patient ability to manage symptoms. 0= can manage extremely well, 10= cannot manage at all
Time frame: Baseline and 6 week follow up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Change From Baseline in Symptom Distress/Symptom Management | Symptom Distress: 6 week follow up | 4.2 score on a scale |
| HEART Patients | Change From Baseline in Symptom Distress/Symptom Management | Symptom Management: Baseline | 2.5 score on a scale |
| HEART Patients | Change From Baseline in Symptom Distress/Symptom Management | Symptom Management: Baseline to 6 week follow up visit | 0.2 score on a scale |
| HEART Patients | Change From Baseline in Symptom Distress/Symptom Management | Symptom Management: 6 week follow up | 2.7 score on a scale |
| HEART Patients | Change From Baseline in Symptom Distress/Symptom Management | Symptom Distress: Baseline to 6 week follow up visit | -0.4 score on a scale |
| HEART Patients | Change From Baseline in Symptom Distress/Symptom Management | Symptom Distress: Baseline | 4.6 score on a scale |
| HEART Caregivers | Change From Baseline in Symptom Distress/Symptom Management | Symptom Management: Baseline to 6 week follow up visit | -1.2 score on a scale |
| HEART Caregivers | Change From Baseline in Symptom Distress/Symptom Management | Symptom Distress: Baseline | 5.6 score on a scale |
| HEART Caregivers | Change From Baseline in Symptom Distress/Symptom Management | Symptom Distress: 6 week follow up | 4.3 score on a scale |
| HEART Caregivers | Change From Baseline in Symptom Distress/Symptom Management | Symptom Distress: Baseline to 6 week follow up visit | -1.3 score on a scale |
| HEART Caregivers | Change From Baseline in Symptom Distress/Symptom Management | Symptom Management: Baseline | 3.7 score on a scale |
| HEART Caregivers | Change From Baseline in Symptom Distress/Symptom Management | Symptom Management: 6 week follow up | 2.6 score on a scale |
Change From Baseline in Symptom Severity
MD Anderson Symptom Inventory (MDASI) Head and Neck Module- Includes 13 core items and an additional 9 head and neck cancer module items which calculates a total score of symptom severity. The MDASI assesses the severity of symptoms at their worst in the last 24 hours on a 0-10 Numeric Rating Scale, with 0 being not present and 10 being as bad as you can imagine. Core items and module symptom items are averaged into a mean module severity. A higher score always indicates an increase in severity. A decrease in change from baseline to 6 week follow up indicates improvement of symptoms.
Time frame: Baseline and 6 week follow up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Change From Baseline in Symptom Severity | 6 week follow up visit | 2.0 score on a scale |
| HEART Patients | Change From Baseline in Symptom Severity | Change from baseline to 6 week follow up visit | -1.0 score on a scale |
| HEART Patients | Change From Baseline in Symptom Severity | Baseline | 3.0 score on a scale |
Ease of Mobile App Use/User Engagement
Number of weekly prompt responses missed out of 184 total expected (23 caregivers given 2 prompts per week for 4 weeks).
Time frame: 4 weeks during app use
Population: Measured in Caregivers only. (23 caregivers given 2 prompts per week for 4 weeks= 184 prompts).
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| HEART Patients | Ease of Mobile App Use/User Engagement | 70 number of missed prompts |
Ease of Use/System Usability
System Usability Scale (SUS) - The SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Scores range from 0-100, with higher scores indicating better usability.
Time frame: 6 week follow up visit only (no baseline comparison)
Population: System Usability Scale only measured in Caregivers.
| Arm | Measure | Value (MEAN) |
|---|---|---|
| HEART Patients | Ease of Use/System Usability | 76 score on a scale |
Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health)
PROMIS Scale v1.2 - Global Health short form consists of 10 items that assess overall perceived quality of life and five general domains of health and functioning including overall physical health, mental health, social health, pain, and fatigue. Scoring uses a 5-point Likert scale with the response scores reversed (5=None to 1=Very severe) so that higher scores for responses always indicate better health. Raw scores are summed and converted to a T-score (mean score of 50, SD ± 10), Therefore a person with a T-score of 40 is one SD below the mean. A decrease in the change from baseline to 6 week follow up indicates worsening quality of life, whereas an increase indicates improvement.
Time frame: Baseline and 6 week follow-up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Baseline | 47.7 T-Score |
| HEART Patients | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Change from baseline to 6 week follow up visit | -1.0 T-Score |
| HEART Patients | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | 6 week follow up visit | 46.6 T-Score |
| HEART Caregivers | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Baseline | 49.0 T-Score |
| HEART Caregivers | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Change from baseline to 6 week follow up visit | -0.5 T-Score |
| HEART Caregivers | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | 6 week follow up visit | 48.5 T-Score |
| Patient HRQOL Physical Scores | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | 6 week follow up visit | 44.6 T-Score |
| Patient HRQOL Physical Scores | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Baseline | 42.4 T-Score |
| Patient HRQOL Physical Scores | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Change from baseline to 6 week follow up visit | 2.2 T-Score |
| Caregiver HRQOL Physical Scores | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Baseline | 50.4 T-Score |
| Caregiver HRQOL Physical Scores | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | Change from baseline to 6 week follow up visit | -0.05 T-Score |
| Caregiver HRQOL Physical Scores | Health-Related Quality-of-Life (PROMIS Scale v1.2 - Global Health) | 6 week follow up visit | 50.4 T-Score |
Mean Score of Dyadic Coping/ Dyadic Efficacy
Dyadic Coping was measured using a 5-item cancer-specific subscale version of the Dyadic Coping Inventory. Items are rated on a 5-point scale from 1 (never) to 5 (always). Scores were averaged with a higher score indicating a better outcome. A decrease in change between baseline and 6 week followup visit indicates worsening outcome over time. Dyadic Efficacy is an investigator developed 1-item question How confident are you that you and your loved one can work together as a team to manage the cancer-related problems that come up? Item was answered on a scale of 0 (not at all confident) to 10 (extremely confident), with average score reported. A decrease in change between baseline and 6 week followup visit indicates worsening, where as an increase in change indicates improvement.
Time frame: Baseline and 6 week follow-up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping: Baseline | 4.3 score on a scale |
| HEART Patients | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping: 6 week follow up visit | 4.2 score on a scale |
| HEART Patients | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping: Change from baseline to 6 week follow up | -0.2 score on a scale |
| HEART Patients | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Efficacy: Baseline | 9.0 score on a scale |
| HEART Patients | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Efficacy: 6 week follow up visit | 8.3 score on a scale |
| HEART Patients | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Efficacy: Change from baseline to 6 week follow up | -0.6 score on a scale |
| HEART Caregivers | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Efficacy: 6 week follow up visit | 8.6 score on a scale |
| HEART Caregivers | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping: Baseline | 4.1 score on a scale |
| HEART Caregivers | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Efficacy: Baseline | 8.2 score on a scale |
| HEART Caregivers | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping: 6 week follow up visit | 4.1 score on a scale |
| HEART Caregivers | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Efficacy: Change from baseline to 6 week follow up | 0.4 score on a scale |
| HEART Caregivers | Mean Score of Dyadic Coping/ Dyadic Efficacy | Dyadic Coping: Change from baseline to 6 week follow up | 0.0 score on a scale |
Mean Score of Self-Efficacy
Based on the National Cancer Institute Follow-up Care Use Among Survivors (FOCUS) survey, two questions were asked: How confident are you that you can get advice or information related to your/your loved one's cancer if you needed at this time? and How confident are you that you can (assist your loved one to) keep to the follow-up care schedule recommended by your doctors? Participants rated items on a 5-point Likert scale where 0=Not at all confident to 4= Completely confident. Scores were averaged for each question, whereby higher scores indicated higher level of confidence. Change from baseline to 6 week follow up is also reported. Negative change indicates decline in self-efficacy.
Time frame: Baseline and 6 week follow-up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Mean Score of Self-Efficacy | 6 week f/u Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care | 3.2 score on a scale |
| HEART Patients | Mean Score of Self-Efficacy | Baseline- Self Efficacy: adhering to recommended follow up care | 3.6 score on a scale |
| HEART Patients | Mean Score of Self-Efficacy | Baseline- Self Efficacy: confidence in obtaining cancer related advice | 3.3 score on a scale |
| HEART Patients | Mean Score of Self-Efficacy | 6 week f/u visit- Self Efficacy: adhering to recommended follow up care | 3.6 score on a scale |
| HEART Patients | Mean Score of Self-Efficacy | Change- Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care | -0.1 score on a scale |
| HEART Patients | Mean Score of Self-Efficacy | Change - Self Efficacy: adhering to recommended follow up care | 0.0 score on a scale |
| HEART Caregivers | Mean Score of Self-Efficacy | Change - Self Efficacy: adhering to recommended follow up care | 0.1 score on a scale |
| HEART Caregivers | Mean Score of Self-Efficacy | Baseline- Self Efficacy: confidence in obtaining cancer related advice | 3.0 score on a scale |
| HEART Caregivers | Mean Score of Self-Efficacy | 6 week f/u Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care | 2.8 score on a scale |
| HEART Caregivers | Mean Score of Self-Efficacy | Change- Self Efficacy: confidence in obtaining cancer related advice/adhering to follow up care | -0.2 score on a scale |
| HEART Caregivers | Mean Score of Self-Efficacy | Baseline- Self Efficacy: adhering to recommended follow up care | 3.3 score on a scale |
| HEART Caregivers | Mean Score of Self-Efficacy | 6 week f/u visit- Self Efficacy: adhering to recommended follow up care | 3.4 score on a scale |
Mean Score of Survivorship Readiness/Caregiver Preparedness
The 11-item Preparing for Life As a New Survivor (PLANS) Knowledge Subscale, developed at the University of Michigan, is utilized to evaluate survivor and caregiver (1) knowledge of diagnosis, treatment and side effects, and (2) communication with the cancer team regarding diagnosis, treatment and side effects and 3) preparedness for what to expect over the next year. Items are rated on a 6-point scale where: strongly disagree=1, moderately disagree =2, slightly disagree=3, slightly agree= 4, moderately agree=5 and strongly agree=6. Items were averaged, with a range of 1-6 with higher scores indicating higher levels of agreement.
Time frame: Baseline and 6 week follow-up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Mean Score of Survivorship Readiness/Caregiver Preparedness | Baseline | 4.5 score on a scale |
| HEART Patients | Mean Score of Survivorship Readiness/Caregiver Preparedness | 6 week follow up visit | 4.6 score on a scale |
| HEART Patients | Mean Score of Survivorship Readiness/Caregiver Preparedness | Change from baseline to 6 weeks follow up | 0.1 score on a scale |
| HEART Caregivers | Mean Score of Survivorship Readiness/Caregiver Preparedness | Baseline | 4.6 score on a scale |
| HEART Caregivers | Mean Score of Survivorship Readiness/Caregiver Preparedness | 6 week follow up visit | 4.5 score on a scale |
| HEART Caregivers | Mean Score of Survivorship Readiness/Caregiver Preparedness | Change from baseline to 6 weeks follow up | -0.1 score on a scale |
Mean Score of Unmet Needs
30-item Cancer Survivors/Partners Unmet Needs instruments (CaSUN/ CaSPUN). Needs were endorsed on a yes/no basis, with a range of 0-30 total endorsed needs. A higher score indicates more endorsed needs. Average number of needs is reported.
Time frame: Baseline and 6 week follow up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Mean Score of Unmet Needs | Baseline endorsed needs | 9.5 score on a scale |
| HEART Patients | Mean Score of Unmet Needs | 6 week follow up visit endorsed needs | 8.9 score on a scale |
| HEART Patients | Mean Score of Unmet Needs | Change from baseline to 6 week follow up visit | -0.6 score on a scale |
| HEART Caregivers | Mean Score of Unmet Needs | Baseline endorsed needs | 8.6 score on a scale |
| HEART Caregivers | Mean Score of Unmet Needs | 6 week follow up visit endorsed needs | 7.5 score on a scale |
| HEART Caregivers | Mean Score of Unmet Needs | Change from baseline to 6 week follow up visit | -1.0 score on a scale |
Number of Participants With Care Plan Use Endpoints
Number of participants of use of care plan after session, including patient and caregiver report of Referred to Care Plan again, Used Care Plan, Used educational materials, and Shared Care Plan with others.
Time frame: 6 week follow up visit
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| HEART Patients | Number of Participants With Care Plan Use Endpoints | Used Care Plan | 10 Participants |
| HEART Patients | Number of Participants With Care Plan Use Endpoints | Referred to Care plan again | 17 Participants |
| HEART Patients | Number of Participants With Care Plan Use Endpoints | Used educational materials | 10 Participants |
| HEART Patients | Number of Participants With Care Plan Use Endpoints | Shared Care Plan with others | 7 Participants |
| HEART Caregivers | Number of Participants With Care Plan Use Endpoints | Shared Care Plan with others | 4 Participants |
| HEART Caregivers | Number of Participants With Care Plan Use Endpoints | Referred to Care plan again | 20 Participants |
| HEART Caregivers | Number of Participants With Care Plan Use Endpoints | Used Care Plan | 8 Participants |
| HEART Caregivers | Number of Participants With Care Plan Use Endpoints | Used educational materials | 16 Participants |
Percentage of Participants Rating App Satisfaction/ Perceived Importance
Ratings of satisfaction with app and prompts on a 6 point descriptive rating scale ranging from strongly agree to strongly disagree. Measurements reported below are count of participants who moderately or strongly agreed with individual prompts.
Time frame: 6 week follow up visit
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| HEART Patients | Percentage of Participants Rating App Satisfaction/ Perceived Importance | App support received helped you provide care for your loved one | 17 Participants |
| HEART Patients | Percentage of Participants Rating App Satisfaction/ Perceived Importance | App provided practical tips | 10 Participants |
| HEART Patients | Percentage of Participants Rating App Satisfaction/ Perceived Importance | App support was helpful emotionally | 15 Participants |
| HEART Patients | Percentage of Participants Rating App Satisfaction/ Perceived Importance | Amount of app information was appropriate | 15 Participants |
| HEART Caregivers | Percentage of Participants Rating App Satisfaction/ Perceived Importance | Amount of app information was appropriate | 16 Participants |
| HEART Caregivers | Percentage of Participants Rating App Satisfaction/ Perceived Importance | App support received helped you provide care for your loved one | 13 Participants |
| HEART Caregivers | Percentage of Participants Rating App Satisfaction/ Perceived Importance | App support was helpful emotionally | 11 Participants |
| HEART Caregivers | Percentage of Participants Rating App Satisfaction/ Perceived Importance | App provided practical tips | 12 Participants |
Process Monitoring Data
Resources needed: Session length overall, length of nursing portion of session, length of app training- number of minutes
Time frame: After session completion
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | Process Monitoring Data | Length of full session | 51 minutes |
| HEART Patients | Process Monitoring Data | Length of nursing visit (within full session) | 13 minutes |
| HEART Patients | Process Monitoring Data | Length of App Training | 12 minutes |
PROMIS Depression- Short Form (SF) v1.0 Form 8A
PROMIS Depression- SF v1.0 form 8A is an 8-item Patient-Reported Outcomes Measure Information System (PROMIS) short-form instrument. Respondents are asked how often in the past 7 days they have experienced specific depression symptoms, using a 5-point ordinal rating scale of Never, Rarely, Sometimes, Often, and Always whereby a higher score indicates higher depression. Raw score totals are converted to an item response theory-based T-scores. The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10 with a range of 38.2 to 81.3. Therefore, a person with a T-score of 40 is one SD below the mean. A decrease in change from baseline to 6 week followup indicates reduced depression.
Time frame: Baseline and 6 week follow-up visit
| Arm | Measure | Group | Value (MEAN) |
|---|---|---|---|
| HEART Patients | PROMIS Depression- Short Form (SF) v1.0 Form 8A | Baseline | 51.2 T-Score |
| HEART Patients | PROMIS Depression- Short Form (SF) v1.0 Form 8A | 6 week follow up visit | 48.0 T-Score |
| HEART Patients | PROMIS Depression- Short Form (SF) v1.0 Form 8A | Change from baseline to 6 week follow up visit | -3.2 T-Score |
| HEART Caregivers | PROMIS Depression- Short Form (SF) v1.0 Form 8A | Baseline | 51.1 T-Score |
| HEART Caregivers | PROMIS Depression- Short Form (SF) v1.0 Form 8A | 6 week follow up visit | 49.6 T-Score |
| HEART Caregivers | PROMIS Depression- Short Form (SF) v1.0 Form 8A | Change from baseline to 6 week follow up visit | -1.5 T-Score |