Clinical trial · Interventional
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
NCT04874584CI-TRIAL-00066883completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Chemotherapy Effect | — | UNRESOLVED | — |
| Dehydration | — | UNRESOLVED | — |
| Quality of Life | — | UNRESOLVED | — |
| Self Efficacy | — | UNRESOLVED | — |
| Symptom Cluster | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CTNSM | Behavioral | — | UNRESOLVED |
| Standard of Care Chemotherapy Education | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- CTNSM Group
- description
- Culturally Tailored Nurse Symptom Management group (CTNSM) - participants in the CTNSM group will receive one in-person or telehealth face-to-face education session followed by a weekly telephone call and/or text message during the first 12 weeks of standard of care chemotherapy. In addition, participants can receive standard of care chemotherapy education.
- interventionNames
- Behavioral: CTNSM
- Behavioral: Standard of Care Chemotherapy Education
- type
- ACTIVE_COMPARATOR
- label
- Standard of Care (control) Group
- description
- Participants in the control group will only be receiving the standard of care chemotherapy education.
- interventionNames
- Behavioral: Standard of Care Chemotherapy Education
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.