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This study is being done to determine if it is possible to incorporate spiritual care sessions as part of the care plan for patients hospitalized for leukemia treatment. In this study, participants will be randomly assigned to either no intervention (standard, real world inpatient spiritual care) or to receive study-specific guided spiritual sessions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Spiritual Intervention Arm | Experimental | Participants receive a study specific spiritual care intervention. |
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| No Intervention Arm | No Intervention |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SCORE Intervention | Behavioral | Participants assigned to this arm will receive regularly scheduled visits from the study spiritual care team during their hospital admission (four times within 14 days). |
| Measure | Description | Time Frame |
|---|---|---|
| Is it feasible to enroll patients to a spiritual intervention study? | Study will compare the number of potential participants to those that enroll and complete 3 out of 4 study intervention sessions. | End of study (approximately 2 years) |
| Will patients accept using the study specific spiritual intervention? | This will be measured on using the Lothian Chaplaincy Patient Reported Outcome Measure (PROM) questionnaire. This measures patient feelings related to spiritual care using rating from not at all to all of the time. | End of study (approximately 2 years) |
| Measure | Description | Time Frame |
|---|---|---|
| Improvement on Patient Reported Spiritual Wellness | This will be measured by improvement (higher scores) reported by participants on the Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being 12 Item Scale (FACIT-sp12) questionnaire. | End of study (approximately 2 years) |
| Improvement on Patient Reported Quality of Life |
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Inclusion criteria
Exclusion criteria
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Clinical Trials Intake | Contact | 1-855-702-8222 | cancerclinicaltrials@bsd.uchicago.edu |
| Name | Affiliation | Role |
|---|---|---|
| Wendy Stock | University of Chicago | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UChicago Medicine Comprehensive Cancer Center | Recruiting | Chicago | Illinois | 60637 | United States |
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| ID | Term |
|---|---|
| D007938 | Leukemia |
| ID | Term |
|---|---|
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
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This will be measured by improvement (higher scores) reported by participants on the Functional Assessment of Cancer Therapy - Leukemia (FACT-Leu) questionnaire. |
| End of study (approximately 2 years) |
| Improvement on Patient Reported Mood | This will be measured by improvement (lower scores) reported by participants on the Hospital Anxiety and Depression Scale (HADS) questionnaire. | End of study (approximately 2 years) |