Trial · NCT03375489
Outcomes16
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 16 of 16
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Patient-reported Quality of Life | 24 Weeks | The analysis population represents the numbers of patients in each study group who completed the baseline and 24-week Functional Assessment of Cancer Therapy - Lung Questionnaire. | units on a scale | LEAST_SQUARES_MEAN |
| SECONDARY | Patient-reported Communication About Their End-of-Life Care Preferences With Their Clinicians | 48 weeks (or last assessment prior to death if before 48 weeks) | The analysis population represents the numbers of patients in each study group who completed the Prognosis and Treatment Perceptions Questionnaire at least once post baseline up to 48 weeks. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Length of Stay in Hospice | From hospice enrollment until patient death during study period | The analysis population represents the numbers of patients in each study group who who died during the study period. | days | LEAST_SQUARES_MEAN |
| SECONDARY | Proportion of Patient's Palliative Care Visits With a Caregiver Present | 24 weeks | The analysis population represents the numbers of patients in each study group who had any palliative care visits, and the overall number of units analyzed represents the numbers of palliative care visits in each study group through week 24. | proportion of visits with a caregiver | NUMBER |
| SECONDARY | Patient-reported Satisfaction With Care | 24 weeks | The analysis population represents the numbers of patients in each study group who completed the 24-week Satisfaction and Care Delivery Questionnaire. | units on a scale | LEAST_SQUARES_MEAN |
| SECONDARY | Caregiver-reported Satisfaction With Care | 24 weeks | The analysis population represents the numbers of caregivers in each study group who completed the 24-week Satisfaction and Care Delivery Questionnaire. | units on a scale | LEAST_SQUARES_MEAN |
| OTHER_PRE_SPECIFIED | Patient-reported Coping Strategies | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Patient-reported Prognostic Understanding | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Caregiver-reported Prognostic Understanding | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Caregiver-reported Quality of Life | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Caregiver-reported Mood Symptoms | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Patient-reported Mood Symptoms | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Patient-reported Depression | up to 48 weeks | |||
| OTHER_PRE_SPECIFIED | Health Care Utilization | Through study completion, average of 18 month follow up | |||
| OTHER_PRE_SPECIFIED | Caregiver-reported Quality of Patient Death | Up to 6 months after patient death during study period | |||
| OTHER_PRE_SPECIFIED | Patient-reported Quality of Life | up to 48 weeks |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT03375489/outcomes