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Culturally Tailored Nurse Coaching Study for Cancer Symptom Management

Utilizing a Culturally Tailored Nurse Coaching Intervention to Decrease Symptom Severity and Prevent Dehydration in Patients With Metastatic Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04874584
Enrollment
34
Registered
2021-05-05
Start date
2021-10-27
Completion date
2023-05-31
Last updated
2023-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chemotherapy Effect, Dehydration, Quality of Life, Self Efficacy, Symptom Cluster

Keywords

symptom self-management, symptom severity, emotional support

Brief summary

The purpose of the study is to see whether or not a telephone/ text message intervention, delivered by a registered nurse, is helpful in managing symptoms and can also prevent dehydration caused by chemotherapy treatment when given together for patients with metastatic breast, colon, lung or prostate cancer.

Interventions

BEHAVIORALCTNSM

The Culturally Tailored Nurse-delivered telephone/text message symptom-management intervention (CTNSM) intervention is an in-person or telehealth face-to-face education session followed by a weekly telephone call and/or text message conducted for the first 12 weeks of standard of care chemotherapy .

BEHAVIORALStandard of Care Chemotherapy Education

Standard of Care chemotherapy education is a one-time patient education session about general treatment-related side effects patients can experience from chemotherapy and the interventions to mitigate the symptoms.

Sponsors

Oncology Nursing Society
CollaboratorOTHER
University of Miami
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Eligible for Chemotherapy for the first time (Previous & Ongoing hormonal only treatment allowed OR Neoadjuvant & Adjuvant chemotherapy regimens with 2+ drugs allowed) 2. \> 18 years old 3. Eastern Cooperative Oncology Group (ECOG) performance status 0-2. 4. There are no life expectancy restrictions 5. Women of child-bearing potential are allowed in the study as long as they are eligible for the chemotherapy treatment. 6. Ability to understand and the willingness to sign a written informed consent document.

Exclusion criteria

1. Patients on immunotherapy only will be excluded 2. Previous chemotherapy 3. Under 18 years old 4. Medically Diagnosed with a Cognitive Impairment. Rationale for excluding people with cognitive impairment is that they would not be able to fully participate in the self-management care aspects of the intervention via the telephone, nor provide informed consent. 5. No access to a telephone 6. Blind or Deaf; If subject is Hearing-impaired or illiterate, then the subject may have a family member participate as a telecommunication surrogate with them in the study

Design outcomes

Primary

MeasureTime frameDescription
Change in MDASI scoresbaseline, up to 12 weeksMD Anderson Symptom Inventory (MDASI) is a 19 item scale with a score range from 0-10 per symptom question that measures symptom severity plus symptom interference combined to measure total symptom burden. The higher score indicates worsening of symptoms.
Incidents of dehydrationup to 12 weeksIncidents of unscheduled medical visits for IV hydration

Secondary

MeasureTime frameDescription
Percentage of completed call or text messageup to 12 weeksFeasibility will be reported as a percentage of completed calls or text messages.
Change in FACT-B Scoresbaseline, up to 12 weeksHealth Related Quality of Life (HRQoL) will be measured by the Functional Assessment of Cancer Therapy -Breast (FACT-B). FACT-B has a total scoring of 0-148 with the higher scoring indicating better HRQoL.
change in Chronic Disease Self-Efficacy Scale (CDSES) scoresbaseline, up to 12 weeksThe CDSES is a 10 item scale with a score range from 0-10 per symptom question that measures perceived self-efficacy. The higher score indicates better perceived self-efficacy.
Change in FACT-C Scoresbaseline, up to 12 weeksHealth Related Quality of Life (HRQoL) will be measured by the Functional Assessment of Cancer Therapy -Colon (FACT-C). FACT-C has a total scoring of 0-144 with the higher scoring indicating better HRQoL.
Change in FACT-LC Scoresbaseline, up to 12 weeksHealth Related Quality of Life (HRQoL) will be measured by the Functional Assessment of Cancer Therapy -Lung Cancer (FACT-LC). FACT-LC has a total scoring of 0-144 with the higher scoring indicating better HRQoL.
Change in FACT-P Scoresbaseline, up to 12 weeksHealth Related Quality of Life (HRQoL) will be measured by the Functional Assessment of Cancer Therapy -Prostate (FACT-P). FACT-P has a total scoring of 0-156 with the higher scoring indicating better HRQoL.
change in Partners in Health Scale (PIHS) scoresbaseline, up to 12 weeksThe PIHS is a 12 item scale with a score range from 0-8 per question that measures symptoms self-management. The higher score indicates better symptom self-management.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026