Metastatic Cancer Clinical Trial
Official title:
Feasibility, Acceptability and Preliminary Effects of the Spiritual Care Assessment and Intervention (SCAI) Framework for Adults With Advanced Cancer and Their Caregivers (FCGs): A Clinical Pilot Trial
Verified date | February 2020 |
Source | Indiana University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to test a spiritual care intervention for adults with advanced cancer and their caregivers. This intervention will assess 4 areas of spiritual experience: meaning and purpose, relationships, transcendence and peace, self-worth and identity. Participants will be asked to complete questionnaires and participate in 4 sessions with research chaplains.
Status | Completed |
Enrollment | 42 |
Est. completion date | August 28, 2019 |
Est. primary completion date | August 28, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patient is at least 18 years of age. - Patient is at least 2 weeks post-diagnosis of an incurable and advanced stage (IV) lung, colorectal, GI neuroendocrine and Hepatobiliary, testicular and esophageal solid malignancy and receiving cancer care at IU Simon Cancer Center. - Patient is willing and able to consent, has a reliable phone and willing to participate in 4 sessions of 30 (+/- 5) minutes per session. - Patient has a family member or eligible friend considered to be a caregiver and interested in participating in the study. - Patient has adequate English fluency for completion of data collection. - Family Caregiver (FCG) is at least 18 years of age. - Family Caregiver (FCG) has been invited to participate in the trial with a patient who meets eligibility criteria above. - Family Caregiver (FCG) is willing and able to consent and to participate in 4 sessions of 30 (+/- 5) minutes per session - Family Caregiver (FCG) has adequate English fluency for completion of data collection. Exclusion Criteria: - Patient makes 3 or more errors on a validated 6-item cognitive screener (Appendix A) or exhibits significant psychiatric or cognitive impairment (e.g., dementia/delirium, retardation, active psychosis) that in the judgment of the investigators would preclude providing informed consent and study participation. - Currently receiving hospice care (patients who enroll in hospice during the trial will have the option of continuing trial participation). - Family Caregiver (FCG) exhibits significant psychiatric or cognitive impairment (e.g., dementia/delirium, retardation, active psychosis) that in the judgment of the investigators would preclude providing informed consent and study participation. |
Country | Name | City | State |
---|---|---|---|
United States | Indiana University Melvin & Bren Simon Cancer Center | Indianapolis | Indiana |
Lead Sponsor | Collaborator |
---|---|
Indiana University | Indiana University Health |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of enrollment | number of eligible patients that are consented and enrolled in the trial | from recruitment to enrollment (i.e. up to 30 days) | |
Primary | Attendance Rate | proportion of participants who attend all four intervention sessions | 4 weeks | |
Primary | Mean Satisfaction Score | satisfaction score among participants on the satisfaction survey | 4 weeks | |
Primary | Functional assessment of chronic illness therapy—Spiritual Well-being Scale Scores | Total score at baseline will be compared to score at to the score at 1 week, 6 weeks, and 3 months | baseline, 1-2 weeks after session 4, 6 weeks, 3 months | |
Secondary | Percentage of completed baseline surveys | percentage of completed baseline surveys in enrolled patients | baseline | |
Secondary | Percentage of completed follow up surveys | baseline, 1-2 weeks after session 4, 6 weeks, 3 months | ||
Secondary | McGrill Quality of Life Questionnaire score | Measure of patient quality of life through total score at baseline compared to score at 1 week, 6 weeks, and 3 months | baseline, 1-2 weeks after session 4, 6 weeks, 3 months | |
Secondary | Caregiver Quality of Life Index-Cancer Questionnaire score | Measure of caregiver quality of life through total score at baseline compared to score at 1 week, 6 weeks, and 3 months | baseline, 1 week, 6 weeks, 3 months | |
Secondary | Caregiver Quality of Life Index-Cancer Questionnaire score | Measure of caregiver quality of life through total score at baseline compared to score at 1 week, 6 weeks, and 3 months | baseline, 1-2 weeks after session 4, 6 weeks, 3 months | |
Secondary | Generalized Anxiety Disorder Scale Scores | Measure of Anxiety through total score at baseline compared to score at 1 week, 6 weeks, and 3 months | baseline, 1-2 weeks after session 4, 6 weeks, 3 months | |
Secondary | Patient Health Questionnaire Depression Scale (PHQ-8) | Measure of depression through total score at baseline compared to score at 1 week, 6 weeks, and 3 months | baseline, 1 week, 6 weeks, 3 months | |
Secondary | Brief RCOPE score | Measure of coping through total score at baseline compared to score at 1 week, 6 weeks, and 3 months | baseline, 1-2 weeks after session 4, 6 weeks, 3 months | |
Secondary | Intervention Satisfaction Questionnaire score | baseline, 1-2 weeks after session 4, 6 weeks, 3 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05094804 -
A Study of OR2805, a Monoclonal Antibody Targeting CD163, Alone and in Combination With Anticancer Agents
|
Phase 1/Phase 2 | |
Enrolling by invitation |
NCT00068003 -
Harvesting Cells for Experimental Cancer Treatments
|
||
Recruiting |
NCT05798611 -
Study of ART0380 in Patients With Biologically Selected Solid Tumors
|
Phase 2 | |
Not yet recruiting |
NCT04931420 -
Study Comparing Standard of Care Chemotherapy With/ Without Sequential Cytoreductive Surgery for Patients With Metastatic Foregut Cancer and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid Levels
|
Phase 2 | |
Recruiting |
NCT05566574 -
A Study of RP-3500 in Combination With Standard Radiation Therapy in People With Solid Tumor Cancer
|
Phase 1/Phase 2 | |
Recruiting |
NCT05036681 -
A Phase II Study of Futibatinib and Pembrolizumab in Metastatic Microsatellite Stable Endometrial Carcinoma
|
Phase 2 | |
Withdrawn |
NCT00005030 -
SCH 66336 Before Surgery in Treating Patients With Colorectal Cancer That Has Metastasized to the Liver
|
Phase 1 | |
Recruiting |
NCT05525858 -
KPMNG Study of MOlecular Profiling Guided Therapy Based on Genomic Alterations in Advanced Solid Tumors II
|
||
Recruiting |
NCT04085029 -
Role of Ablative Radiotherapy in the Management of Metastatic Disease: A Patient Data Registry
|
||
Recruiting |
NCT06058988 -
Trastuzumab Deruxtecan (T-DXd) for People With Brain Cancer
|
Phase 2 | |
Not yet recruiting |
NCT05981170 -
Rurality Adapted Physical Activity Sport Health
|
||
Not yet recruiting |
NCT03058809 -
Evaluation of Viatarâ„¢ Oncopheresis System in Removing CTC From Whole Blood
|
Phase 1/Phase 2 | |
Completed |
NCT02529553 -
A Study of LY3076226 in Participants With Advanced or Metastatic Cancer
|
Phase 1 | |
Terminated |
NCT01929941 -
An Open-Label Study of a Novel JAK-inhibitor, INCB047986, Given in Patients With Advanced Malignancies
|
Phase 1 | |
Completed |
NCT01302808 -
Romidepsin and Erlotinib Hydrochloride in Treating Patients With Stage III or Stage IV Non-Small Cell Lung Cancer
|
Phase 1 | |
Terminated |
NCT00918645 -
Calcium-41 (41Ca) Chloride Aqueous Solution in Diagnosing Patients With Prostate Cancer and Bone Metastasis
|
N/A | |
Completed |
NCT00795678 -
Chemotherapeutic Agents in Brain/Breast
|
N/A | |
Withdrawn |
NCT00769990 -
Genistein in Treating Patients Undergoing External-Beam Radiation Therapy for Bone Metastases
|
Phase 1/Phase 2 | |
Completed |
NCT00557102 -
Cetuximab and Combination Chemotherapy as First-Line Therapy in Treating Patients With Colorectal Cancer That Has Spread to the Liver and/or Lung
|
Phase 2 | |
Recruiting |
NCT00398437 -
Magnetic Resonance Imaging for the Early Detection of CNS Metastases in Women With Stage IV Breast Cancer
|
N/A |