Clinical trial · Observational
Investigating the Feasibility and Acceptability of an Innovative Interdisciplinary Supportive Care Program: Couples Coping Together Against Cancer
NCT07664579CI-TRIAL-00115691recruitingClinicalTrials.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)
This study evaluates how useful and acceptable the components of the "Couples Coping Together Against Cancer", referred to as "The Program", are to the participants with 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 |
|---|---|---|---|
| Anatomic Stage IV Breast Cancer AJCC v8 | — | UNRESOLVED | — |
| Glioblastoma | Glioblastoma | CURATED_BROADER | 0.80 |
| Lung Carcinoma | Lung Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Malignant Solid Neoplasm | Malignant Solid Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Metastatic Breast Carcinoma | Breast Carcinoma | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Non-Interventional Study | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Observational
- description
- Patient and partners receive access to the Connecting Care App tool and undergo biopsychosocial screening and psychoeducation sessions over 30-45 minutes and complete surveys on study. Patients and partners may also receive counseling sessions over 30-45 minutes for up to 4 sessions on study.
- interventionNames
- Other: Non-Interventional Study
Primary outcomes (4)
- measure
- Accrual rate (AR)
- timeFrame
- Up to 12 months
- description
- Defined as number of enrolled dyads/number of eligible dyads x 100. Recruitment rate along with 95% confidence interval (CI) will be calculated. Program will be considered feasible with ≥ 70% recruitment rate.
- measure
- Retention rate (RR)
- timeFrame
- At 3 month and 6 month follow up
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Have received a diagnosis of a primary brain tumor (glioblastoma), or other cancers (breast, lung, etc.) * Are new patients to City of Hope (COH) (all sites) or receive at least some of their care at City of Hope- Duarte Campus (care is defined as: procedures, consults, laboratories, imaging, surgery, and/or treatment) * The patient is in a committed relationship/partnership with a partner and the partner is available and willing to participate * Are English or Spanish speaking * ≥ 18 years of age * Have access to a smartphone, computer/laptop or internet connection to complete all study procedures Exclusion Criteria: * Significant cognitive impairment * Inpatient psychiatric treatment for severe mental illness or overt signs of severe psychopathology (e.g., psychosis) * Visual, hearing, voice, or motor impairment that prevents completion of study procedures as evidenced by clinical judgment * Committed partners will be excluded from the study if they: * Refuse to complete informed consent * Have cognitive impairment * Have severe mental illness that would prevent informed consent and completion of study activities as evidenced by clinical judgment
References
Publications (0)
Data not yet available
No reference posted for this study.