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| ID | Type | Description | Link |
|---|---|---|---|
| CSDG-24-1319592-01-CTPS | Other Grant/Funding Number | American Cancer Society Clinician Scientist Development Grant (CSDG) |
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| Name | Class |
|---|---|
| American Cancer Society, Inc. | OTHER |
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The goal of this study is to develop a virtual group intervention to address post-traumatic stress related to cancer in young adult cancer survivors (YACs, aged 18-39). The study team will do this by integrating evidence-guided treatments and expert clinician feedback (N=10) on the content, delivery, and structure of the intervention. Next, the study team will refine this intervention through a pilot trial with a group of YACs (N=80).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Psychosocial Intervention for Cancer-Related Post-Traumatic Stress in Young Adults | Experimental | The study team aims to evaluate the feasibility and acceptability of the adapted psychosocial intervention through a pilot trial with a group of 80 YACs, followed by mixed-methods data analysis of feasibility and acceptability outcomes. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Psychosocial Intervention for Cancer-Related Post-Traumatic Stress in Young Adults | Behavioral | A new group-based virtual intervention to address post-traumatic stress related to cancer in YACs, integrating evidence-guided treatments from Cognitive Processing Therapy and Mind-Body Resiliency interventions. |
| Measure | Description | Time Frame |
|---|---|---|
| Intervention Feasibility: Percent of Identified Prospective Participants Who Enroll | Percent of eligible participants who were offered participation and who enroll in the study by completing consent and baseline assessment. | Post-treatment completion (enrollment to treatment completion is approximately 3 months) |
| Intervention Feasibility: Proportion of Participants Completing the Program | Percent of enrolled participants who complete the program, defined as completing 6 out of 8 sessions. | Post-treatment completion (enrollment to treatment completion is approximately 3 months) |
| Intervention Acceptability | Acceptability will be assessed by the Client Satisfaction Questionnaire (CSQ-8). The intervention study will be considered acceptable if ≥80% of participants rate it as acceptable (defined as a CSQ-8 score ≥20). | Post-treatment completion (enrollment to treatment completion is approximately 3 months) |
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Inclusion Criteria: To be eligible for this study, participants will be:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Zeba N Ahmad, Ph.D. | Contact | 617-724-1586 | zahmad2@mgh.harvard.edu | |
| Xinghan Zhu, B.S. | Contact | 617-724-7593 | xzhu@mgh.harvard.edu |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mass General Cancer Center | Boston | Massachusetts | 02114 | United States |
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| ID | Term |
|---|---|
| D000083626 | Psychosocial Intervention |
| ID | Term |
|---|---|
| D011613 | Psychotherapy |
| D004191 | Behavioral Disciplines and Activities |
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