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NCT02660996

Effectiveness of the Advocate Lutheran General Survivorship Center Programs

Completed Last updated 4 October 2024
What this trial tests

trial in Cancer in 22 participants. Completed in 14 August 2017.

Timeline
1 October 2016
Primary endpoint
31 March 2017
14 August 2017

Quick facts

Lead sponsorWake Forest University Health Sciences
StatusCompleted
Study typeOBSERVATIONAL
Enrollment22
Start date1 October 2016
Primary completion31 March 2017
Estimated completion14 August 2017
Sites1 location across United States

Conditions studied

Sponsor

Wake Forest University Health Sciences

Who can join

18 and older, any sex, with Cancer or Quality of Life. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this observational study is to assess the effectiveness of the Advocate Lutheran General Survivorship Center's Programs by measuring the following outcomes of interest on participating patients: 1. Quality of life 2. Distress level 3. Satisfaction with the Survivorship Program General Hypothesis: Patients who participate in at least four classes in a two month period will have higher scores on the post-class satisfaction, quality of life, and distress surveys compared to their pre-class surveys.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Cancer

Currently open trials in the same condition.

Other Wake Forest University Health Sciences trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02660996.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing