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Enhancing Self Care Among Oral Cancer Survivors: The Empowered Survival Trial

Primary Purpose

Oral Cancer, Oropharyngeal Cancer, Head and Neck Cancer

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Empowered Survivor Online
Springboard Beyond Cancer
Survey Administration
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Oral Cancer

Eligibility Criteria

18 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age > 18 years;
  • Diagnosed with a first primary invasive oral or oropharyngeal cancer between 1 and 3 years ago;
  • Currently cancer free (but can have experienced a recurrence);
  • Has internet access;
  • Read English;
  • Has sufficient vision to read a survey and complete an online intervention

Exclusion Criteria:

-

Sites / Locations

  • Rutgers Cancer Institute of New JerseyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Empowered Survivor online

Springboard Beyond Cancer

Arm Description

The online intervention, called Empowered Survivor (ES) is a self-management intervention for patients with head and neck cancer. The intervention contains the following modules: Introduction; Difficulty Swallowing and Muscle Strength; Oral Care; Long-term Follow-Up Care/Oral exams; Calm and Connect; and Maintaining.

Springboard Beyond Cancer is a general resource for survivors of all cancer. It is a free self-management program for cancer survivors developed by trusted sources, the ACS and the NCI.

Outcomes

Primary Outcome Measures

Self-efficacy score
Change in self- efficacy measured with the Self-efficacy scale (22 items) which targets confidence in managing aspects of self-care (e.g., dry mouth, swallowing, oral self-exam, communicating with providers, emotions). Administered at multiple time points to measure effect of the intervention. Ratings range from 1 (not at all confident) to 5 (very confident). An item average will be calculated.
Preparedness for survivorship
Change in preparedness for survivorship. The Preparedness for survivorship scale (10 items) developed by the investigator assesses whether information received about survivorship was sufficient, helpful, comprehensive, and covered self-care tasks. Administered at multiple time points to measure effect of the intervention. Items are rated on a 4-point Likert scale (1 = strongly disagree, 4 = strongly agree). Higher score indicate better preparedness.
Quality of Life score measured using the The European Organization for Research and Treatment of Cancer (EORTC)- Head and Neck
Change in QOL score over time. The European Organization for Research and Treatment of Cancer - Quality of Life Questionnaire- Head and Neck-43. The European Organization for Research and Treatment of Cancer - Quality of Life Questionnaire- Head and Neck-43 is the updated version of the EORTC H&N 35, used in the researcher's pilot work. The EORTC QLQ-HN is the most widely-used measure of Head and Neck QOL. The investigators use the total score in analyses, but will evaluate subscales. Administered at multiple time points to measure effect of the intervention. Items are rated on 1 (not at all)-4 (very much) Likert scale and higher scores indicate worse QOL.

Secondary Outcome Measures

Performance of oral self-exam, past month
1 item asking the participant if he/she has performed an oral self-exam, past month. Yes/No. Administered at multiple time points to measure effect of the intervention.
Comprehensiveness is the number of areas checked (11 areas) during the oral self-exam
Change in comprehensiveness of exams over time. 11 items will list the areas to check and ask participant to indicate Yes/No if the participant checked that area during the oral self-exam. Administered at multiple time points to measure effect of the intervention.
Performance of exercises to improve swallowing, past month (yes/no)
One question asking participants if they have completed exercises to improve swallowing in the past month. Administered at multiple time points to measure effect of the intervention.
Performance of head/neck exercises, past month (yes/no)
One question asking participants if they have completed head and neck exercises in the past month. Administered at multiple time points to measure effect of the intervention.

Full Information

First Posted
January 12, 2021
Last Updated
February 6, 2023
Sponsor
Rutgers, The State University of New Jersey
Collaborators
National Cancer Institute (NCI), The Cancer Registry of Greater California, The New Jersey State Cancer Registry
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1. Study Identification

Unique Protocol Identification Number
NCT04713449
Brief Title
Enhancing Self Care Among Oral Cancer Survivors: The Empowered Survival Trial
Official Title
Enhancing Self Care Among Oral Cancer Survivors: The Empowered Survivor Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 19, 2021 (Actual)
Primary Completion Date
March 1, 2025 (Anticipated)
Study Completion Date
March 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
National Cancer Institute (NCI), The Cancer Registry of Greater California, The New Jersey State Cancer Registry

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Project's goal is evaluate an online tool the research team created called Empowered Survivor (ES) against a free online self-management intervention developed for cancer survivors by the National Cancer Institute and the American Cancer Society called Springboard Beyond Cancer.
Detailed Description
600 patients who have completed treatment between one and three years ago and are currently cancer-free will be recruited via the New Jersey State Cancer Registry or the Cancer Registry of Greater California and randomly assigned to ES or Springboard Beyond Cancer. Participants will complete measures at baseline, 2, and 6-months post-baseline. The investigators will also complete a process evaluation of Empowered Survivor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Cancer, Oropharyngeal Cancer, Head and Neck Cancer

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Empowered Survivor online
Arm Type
Experimental
Arm Description
The online intervention, called Empowered Survivor (ES) is a self-management intervention for patients with head and neck cancer. The intervention contains the following modules: Introduction; Difficulty Swallowing and Muscle Strength; Oral Care; Long-term Follow-Up Care/Oral exams; Calm and Connect; and Maintaining.
Arm Title
Springboard Beyond Cancer
Arm Type
Active Comparator
Arm Description
Springboard Beyond Cancer is a general resource for survivors of all cancer. It is a free self-management program for cancer survivors developed by trusted sources, the ACS and the NCI.
Intervention Type
Other
Intervention Name(s)
Empowered Survivor Online
Intervention Description
Informational online intervention for head and neck cancer survivors
Intervention Type
Other
Intervention Name(s)
Springboard Beyond Cancer
Intervention Description
Informational online intervention for all cancer survivors
Intervention Type
Other
Intervention Name(s)
Survey Administration
Intervention Description
Survey measures administered at BL, two and 6 months post-baseline
Primary Outcome Measure Information:
Title
Self-efficacy score
Description
Change in self- efficacy measured with the Self-efficacy scale (22 items) which targets confidence in managing aspects of self-care (e.g., dry mouth, swallowing, oral self-exam, communicating with providers, emotions). Administered at multiple time points to measure effect of the intervention. Ratings range from 1 (not at all confident) to 5 (very confident). An item average will be calculated.
Time Frame
Baseline, two and 6 months post-baseline
Title
Preparedness for survivorship
Description
Change in preparedness for survivorship. The Preparedness for survivorship scale (10 items) developed by the investigator assesses whether information received about survivorship was sufficient, helpful, comprehensive, and covered self-care tasks. Administered at multiple time points to measure effect of the intervention. Items are rated on a 4-point Likert scale (1 = strongly disagree, 4 = strongly agree). Higher score indicate better preparedness.
Time Frame
Baseline, two and 6 months post-baseline
Title
Quality of Life score measured using the The European Organization for Research and Treatment of Cancer (EORTC)- Head and Neck
Description
Change in QOL score over time. The European Organization for Research and Treatment of Cancer - Quality of Life Questionnaire- Head and Neck-43. The European Organization for Research and Treatment of Cancer - Quality of Life Questionnaire- Head and Neck-43 is the updated version of the EORTC H&N 35, used in the researcher's pilot work. The EORTC QLQ-HN is the most widely-used measure of Head and Neck QOL. The investigators use the total score in analyses, but will evaluate subscales. Administered at multiple time points to measure effect of the intervention. Items are rated on 1 (not at all)-4 (very much) Likert scale and higher scores indicate worse QOL.
Time Frame
Baseline, two and 6 months post-baseline
Secondary Outcome Measure Information:
Title
Performance of oral self-exam, past month
Description
1 item asking the participant if he/she has performed an oral self-exam, past month. Yes/No. Administered at multiple time points to measure effect of the intervention.
Time Frame
Baseline, two and 6 months post-baseline
Title
Comprehensiveness is the number of areas checked (11 areas) during the oral self-exam
Description
Change in comprehensiveness of exams over time. 11 items will list the areas to check and ask participant to indicate Yes/No if the participant checked that area during the oral self-exam. Administered at multiple time points to measure effect of the intervention.
Time Frame
Baseline, two and 6 months post-baseline
Title
Performance of exercises to improve swallowing, past month (yes/no)
Description
One question asking participants if they have completed exercises to improve swallowing in the past month. Administered at multiple time points to measure effect of the intervention.
Time Frame
Baseline, two and 6 months post-baseline
Title
Performance of head/neck exercises, past month (yes/no)
Description
One question asking participants if they have completed head and neck exercises in the past month. Administered at multiple time points to measure effect of the intervention.
Time Frame
Baseline, two and 6 months post-baseline
Other Pre-specified Outcome Measures:
Title
Action and Planning Coping
Description
Change in Action and Planning coping score. The scale (8 items) assesses the degree to which a detailed plan is made for self-care tasks. Administered at multiple time points to measure effect of the intervention. Items are rated on a 5-point Likert scale(1 = strongly disagree, 5 = strongly agree). Mean scale score will be reported. Higher score = higher action coping.
Time Frame
Baseline, two and 6 months post-baseline
Title
Patient activation
Description
Change in Patient activation scale score. Patient Activation Scale (13 items) assesses the active role in cancer care. Administered at multiple time points to measure effect of the intervention. Items are rated on a 4-point scale (1 = Disagree strongly, 4 = Agree strongly). Higher score = higher activation.
Time Frame
Baseline, two and 6 months post-baseline
Title
Information Needs
Description
Change in score over time. Information needs (23 items) is adapted from the FOCUS Health-Related Topics measure. Administered at multiple time points to measure effect of the intervention. Participants reported if they would like more information on each topic (yes/no). The number of " yes" responses are averaged.
Time Frame
Baseline, two and 6 months post-baseline
Title
Support needs
Description
Change in Support needs. The support needs scale (34 items) assesses physical, psychological, and health care needs. Administered at multiple time points to measure effect of the intervention. Participants are asked to indicate the extent to which they needed help in the past month (1 = No Need; Not applicable, "This is not a problem",2 = No need; Satisfied, "I did need help but my need was satisfied," 3 = Low need; "It caused me concern and I had little need for additional help," 4 = Moderate need-"It caused me concern and I had some need for additional help," 5 = High need; -"It caused me concern and I had a strong need for additional help"). Support needs that are rated as "moderate"(4) or "high" need (5) will be summed, with a range of 0 to 34.
Time Frame
Baseline, two and 6 months post-baseline
Title
Concerns about recurrence scale
Description
Change in concerns about recurrence. The first 4 items from the concerns about recurrence scale are measured on a 1-6 scale. with lower scores indicating less concerns or worry. The additional 21 items are rated on 0 (not at all) to 4 (extremely) with higher scores indicating more concerns or worry. Administered at multiple time points to measure effect of the intervention.
Time Frame
Baseline, two and 6 months post-baseline
Title
Moderator-Race/ethnicity
Description
Race/ethnicity will be assessed.
Time Frame
Baseline only
Title
Moderator-Receipt of survivorship care plan
Description
Yes/No did the participant receive a survivorship care plan
Time Frame
Baseline only
Title
Moderator- Baseline self-efficacy score
Description
The baseline score on the scale will be (22 items) examined. The scale targets confidence in managing aspects of self-care (e.g., dry mouth, swallowing, oral self-exam, communicating with providers, emotions). Ratings are 1- 5
Time Frame
Baseline Only

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age > 18 years; Diagnosed with a first primary invasive oral or oropharyngeal cancer between 1 and 3 years ago; Currently cancer free (but can have experienced a recurrence); Has internet access; Read English; Has sufficient vision to read a survey and complete an online intervention Exclusion Criteria: -
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sharon Manne, PhD
Phone
732-235-6759
Email
Sharon.Manne@rutgers.edu
Facility Information:
Facility Name
Rutgers Cancer Institute of New Jersey
City
New Brunswick
State/Province
New Jersey
ZIP/Postal Code
08901
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sharon Manne, PhD
Phone
732-235-6759
Email
mannesl@cinj.rutgers.edu
First Name & Middle Initial & Last Name & Degree
Sharon L Manne, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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Enhancing Self Care Among Oral Cancer Survivors: The Empowered Survival Trial

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