- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05645510
LIVInG With chrONic Cancer TrEatments (LONGEVITI) Study (LONGEVITI)
May 6, 2026 updated by: University of Alberta
People with advanced chronic cancers are now living for many years as a result of new targeted anti-cancer treatments.
Many of these treatments are quite new and people may take them for months, even years, as long as the treatments are helping.
The purpose of this study is to help understand how to best support people receiving these treatments.
Study Overview
Status
Recruiting
Detailed Description
Participants ill be scheduled for an in-person, telephone or computer video interview with the researcher(s).
They will be asked about their experiences receiving targeted anti-cancer treatments.
Then over the next 3 months, participants will be asked to think about how receiving these cancer treatments affects daily living and to create a 'metaphor'.
Metaphors may be composed with any mix of visual, verbal, musical or other works participants feel expresses and brings their experiences to life.
Study Type
Observational
Enrollment (Estimated)
75
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Edith Pituskin, PhD
- Phone Number: 7804328221
- Email: pituskin@ualberta.ca
Study Contact Backup
- Name: Meredith Porter Hogg, MN
- Email: lngeviti@ualberta.ca
Study Locations
-
-
Alberta
-
Edmonton, Alberta, Canada, T6G 1C9
- Recruiting
- Edith Pituskin
-
Contact:
- Edith Pituskin, PhD
- Phone Number: 7804328221
- Email: pituskin@ualberta.ca
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
people with cancer taking oral anti-cancer agents over the long term
Description
Inclusion Criteria: taking chronic targeted anti-cancer agents -
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Family-Based
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Interview
Time Frame: 3 months
|
Interview to learn the experiences of people living with incurable cancers
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 24, 2022
Primary Completion (Estimated)
June 9, 2026
Study Completion (Estimated)
June 9, 2026
Study Registration Dates
First Submitted
November 30, 2022
First Submitted That Met QC Criteria
November 30, 2022
First Posted (Actual)
December 9, 2022
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 6, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Genital Diseases
- Endocrine System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Genital Neoplasms, Male
- Urogenital Neoplasms
- Neoplasms by Site
- Genital Diseases, Male
- Prostatic Diseases
- Male Urogenital Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Intestinal Diseases
- Immune System Diseases
- Respiratory Tract Diseases
- Neoplasms by Histologic Type
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Digestive System Diseases
- Gastrointestinal Diseases
- Intestinal Neoplasms
- Rectal Diseases
- Genital Diseases, Female
- Lung Diseases
- Hematologic Diseases
- Endocrine Gland Neoplasms
- Respiratory Tract Neoplasms
- Thoracic Neoplasms
- Colonic Diseases
- Ovarian Diseases
- Adnexal Diseases
- Genital Neoplasms, Female
- Gonadal Disorders
- Skin Diseases
- Breast Diseases
- Lymphoproliferative Disorders
- Immunoproliferative Disorders
- Neuroectodermal Tumors
- Neoplasms, Germ Cell and Embryonal
- Neoplasms, Nerve Tissue
- Neuroendocrine Tumors
- Neoplasms, Plasma Cell
- Hemostatic Disorders
- Paraproteinemias
- Blood Protein Disorders
- Hemorrhagic Disorders
- Nevi and Melanomas
- Skin Neoplasms
- Skin and Connective Tissue Diseases
- Hemic and Lymphatic Diseases
- Neoplasms
- Prostatic Neoplasms
- Lung Neoplasms
- Colorectal Neoplasms
- Ovarian Neoplasms
- Breast Neoplasms
- Multiple Myeloma
- Melanoma
Other Study ID Numbers
- HREBA.CC-22-0196
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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