Improving Nutrition and Physical Activity for Cancer Survivors (Tools To Be Fit) (TTBF)
May 29, 2026 updated by: University of California, San Francisco
Optimizing Intervention Tools to Improve Nutrition and Physical Activity for Cancer Survivors (Tools To Be Fit)
This clinical trial studies the effect of four different intervention components "tools" on body weight, nutrition, and physical activity in cancer survivors.
Studies indicate that people with a history of cancer whose nutrition and physical activity habits are consistent with the American Cancer Society's Nutrition and Physical Activity Guidelines may have longer disease-free survival.
The four different intervention components may help patients with a history of cancer adopt recommended health behaviors after they have completed treatment.
Study Overview
Status
Active, not recruiting
Conditions
Detailed Description
PRIMARY OBJECTIVE:
I. To determine the effect of four candidate intervention components (text messaging, digital health tool kit, health coaching, or support person training), and combinations of the four intervention components, on change cancer survivors' American Cancer Society (ACS) guideline score after 48 weeks of intervention.
SECONDARY OBJECTIVES:
I. To determine the effect of four candidate intervention components (text messaging, digital health tool kit, health coaching, or support person training), and combinations of the four intervention components, on cancer survivors' American Cancer Society (ACS) guideline score after 24 weeks of intervention.
II. To determine the effect of four candidate intervention components, and combinations of the four intervention components, on cancer survivors' intake of fruits and vegetables, whole grains, refined grains, red meat, and processed meats; moderate-to-vigorous physical activity; and body mass index (BMI) after 48 weeks of intervention.
EXPLORATORY OBJECTIVES:
I. To determine the effect of four candidate intervention components (text messaging, digital health tool kit, health coaching, or support person coaching), and combinations of the four intervention components, on cancer survivors' American Cancer Society (ACS) guideline score after 12 weeks of intervention.
II. To describe adherence to each intervention component.
III. To explore the effects of each of the candidate intervention components (text messaging, digital health tool kit, health coaching, support person training) on theoretical constructs (e.g., self-efficacy, outcome expectations, self-monitoring, social support) from 0 to 24 and 48 weeks.
IV. To explore whether sociodemographic (e.g., gender, age, race/ethnicity), clinical (e.g., stage of disease, treatment history, ostomy status, time since diagnosis), and/or psychological/behavioral (e.g., self-efficacy, social support, outcome expectations, depression) factors moderate the intervention components' effects on ACS guideline scores.
VII. To explore change in ACS guideline score in relation to change in fasting insulin, glucose, homeostatic model assessment (HOMA-IR), and inflammatory markers (e.g., Interleukin 6 (IL-6), high-sensitivity C-reactive protein (hs-CRP), Tumor Necrosis Factor alpha (TNF-alpha) for a subset of participants from enrollment to 48 weeks among people with a history of cancer.
VIII. To explore change in ACS guideline score in relation to change in fatigue, depression, and sleep quality from 0 to 24 and 48 weeks among people with a history of cancer.
IX. To explore changes in the ACS guideline score in relation to change in the gut microbiome among a subset of participants with a history of cancer.
X. To describe cancer survivors' 10-year cardiovascular risk using the American Heart Association (AHA) Predicting Risk of cardiovascular disease (CVD) EVENTS (PREVENT) score.
XI. Engage stakeholders to identify opportunities for continued optimization of the intervention and prepare for future implementation.
XII. To explore whether aspects of the social or built environment moderate effects of the intervention components on the ACS guideline score
OUTLINE: All patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer. Patients are randomized to 1 of 16 conditions. Participants who consent to complete an end-of-study interview may be asked to complete the interview up to 24 weeks after the end of the intervention.
CONDITION I: Patients receive text messages and use digital health tool kit for 48 weeks. Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION II: Patients receive text messages and use digital health tool kit for 48 weeks. Patients also receive 13 health coaching sessions over 30 each for 48 weeks.
CONDITION III: Patients receive text messages and use digital health tool kit for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION IV: Patients receive text messages and use digital health tool kit for 48 weeks.
CONDITION V: Patients receive text messages for 48 weeks. Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION VI: Patients receive text messages for 48 weeks. Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks.
CONDITION VII: Patients receive text messages for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION VIII: Patients receive text messages for 48 weeks.
CONDITION IX: Patients use digital health tool kit for 48 weeks. Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION X: Patients use digital health tool kit for 48 weeks. Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks.
CONDITION XI: Patients use digital health tool kit for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION XII: Patients use digital health tool kit for 48 weeks.
CONDITION XIII: Patients receive 13 health coaching sessions over 30 minutes each for 48 weeks. Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION XIV: Patients receive 13 health coaching sessions over 30 minutes each for 48 weeks.
CONDITION XV: Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
CONDITION XVI: Patients receive personal report and booklet only.
Study Type
Interventional
Enrollment (Actual)
353
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
San Francisco, California, United States, 94143
- University of California San Francisco
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
INCLUSION CRITERIA FOR CANCER SURVIVORS:
- >= 18 years of age.
- Diagnosis of bladder, breast, colon, endometrial, kidney (renal cell carcinoma), ovarian, prostate, or rectal cancer.
- Completed all cytotoxic chemotherapy, immunotherapy, targeted therapies, or radiation (if indicated) prior to enrollment. Hormonal treatments are allowed.
- Owns a smart phone that has access to the Internet and can receive daily text messages.
- Able to speak and read English or Spanish
- Have a support person >= 18 years of age who speaks English or Spanish and is willing to provide informed consent and support the participant throughout the study.
- >= 4 weeks since a major surgery to start of intervention (removal of port or catheter (cath) is not major surgery; reversal of ostomy is major surgery and will require at least 4 weeks prior to enrollment).
- Readiness, as determined by the Physical Activity Readiness Questionnaire (PAR-Q). If there are any indications that home-based exercise might be unsafe based on PAR-Q, the patient will not be enrolled until confirmation from the patient's provider is received via email and/or phone that they are safe to exercise. Providers do not need to be contacted if patients answer 'yes' to 'Is your doctor currently prescribing any medication for your blood pressure or for a heart condition?
INCLUSION CRITERIA FOR SUPPORT PERSONS:
- Identified by a cancer survivor participant who has consented to participate in Tools To Be Fit as their support person.
- 18 years of age or older.
- Speaks and reads English or Spanish.
- Consents to complete two online surveys and four 1-on-1 health coaching calls during the 48 week study.
Exclusion Criteria:
EXCLUSION CRITERIA FOR CANCER SURVIVORS:
- People with potential contraindications to home-based exercise based on the PAR-Q for whom the investigator is unable to obtain physician clearance.
- ACS guideline score of > 4 out of 6 at enrollment based on self-reported diet, BMI, and physical activity. Our screening survey will ask participants to report their height and weight; usual intake of foods in the ACS guidelines (e.g., red and processed meat, fruits, vegetables, grains); and the Godin Leisure Time Exercise Survey.
- Used a physical activity tracker and a diet tracking app for >= 1 week in the past 3 months; these are components of our digital health tool kit.
- Planned major surgery during the study period (removal of port or cath or dermatological procedures excluded)
- Scheduled to receive any form of cancer therapy during the study period with the exception of hormonal treatments, which are allowed.
- History of severe cardiovascular, respiratory or musculoskeletal disease or joint problems that preclude moderate physical activity. Examples include unstable angina, recent myocardial infarction, oxygen-dependent pulmonary disease, and osteoarthritis requiring imminent joint replacement. Moderate arthritis that does not preclude physical activity is not a reason for ineligibility.
- History of psychiatric disorders that would preclude participation in the study intervention (e.g., untreated major depression or psychosis, substance abuse, severe personality disorder) or prevent the patient from giving informed consent.
- Participating in another weight loss, physical activity or dietary intervention clinical trial. Co-enrollment in some trials involving pharmacologic therapy is allowed. Participants are also allowed to pursue weight loss and physical activity programs on their own, as long as these programs are not provided as part of a clinical trial.
- Currently pregnant or trying to become pregnant during the study period.
- Living outside the United States during screening and/or the 48-week study period.
EXCLUSION CRITERIA FOR SUPPORT PERSONS:
1. None.
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
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Condition IV (text, health kit)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages and use digital health tool kit for 48 weeks.
|
Receive text messages
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition VIII (text)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages for 48 weeks.
|
Receive text messages
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition XII (health kit)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients use digital health tool kit for 48 weeks.
|
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition XVI (study booklet)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
|
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition I (text, health kit, health coach, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages and use digital health tool kit for 48 weeks.
Patients also receive 13 health coaching sessions over 30-45 minutes each for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive health coaching
Other Names:
Receive text messages
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition II (text, health kit, health coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer cancer.
Patients receive text messages and use digital health tool kit for 48 weeks.
Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks.
|
Receive health coaching
Other Names:
Receive text messages
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition III (text, health kit, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages and use digital health tool kit for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive text messages
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition IX (health kit, health coach, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients use digital health tool kit for 48 weeks.
Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive health coaching
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition V (text, health coach, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages for 48 weeks.
Patients also receive 15 health coaching sessions over 30 minutes each for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive health coaching
Other Names:
Receive text messages
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition VI (text, health coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages for 48 weeks.
Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks.
|
Receive health coaching
Other Names:
Receive text messages
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition VII (text, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive text messages for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive text messages
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition X (health kit, health coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients use digital health tool kit for 48 weeks.
Patients also receive 13 health coaching sessions over 30 minutes each for 48 weeks.
|
Receive health coaching
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition XI (health kit, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients use digital health tool kit for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive digital health tool kit
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition XIII (health coach, support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive 13 health coaching sessions over 30 minutes each for 48 weeks.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Receive health coaching
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition XIV (health coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Patients receive 13 health coaching sessions over 30 minutes each for 48 weeks.
|
Receive health coaching
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
|
Experimental: Condition XV (support coach)
Patients receive a personal report comparing their nutrition and physical activity to ACS guidelines and a booklet on nutrition and physical activity for patients with a history of cancer.
Support persons receive four coaching sessions lasting 30 minutes each, approximately every 12 weeks for 48 weeks.
|
Receive support person coaching
Other Names:
Quality of Life and Behavioral Questionnaires
Other Names:
Receive personal report and booklet on nutrition and physical activity for patients with a history of cancer
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean change in American Cancer Society (ACS) guideline score at 48 weeks
Time Frame: Up to 48 weeks
|
The ACS Guideline Score is comprised of scores on participant reported food intake (score range from 0-2), physical activity (score range from 0-2), and body mass index (BMI) (score range from 0-2).
The total score is calculated by summing the scores on each component with a total score range from 0 to 6. Greater scores indicate a greater level of healthy choices made by the participant.
The investigator will assess the independent and interaction effects of the four treatment components on change in ACS score as repeated measures and using a generalized linear mixed effect model, starting with the saturated model, including coefficients for main effects, interactions up to 3-way, and stratification variables (gender and age), and reduce the model via backward variable selection with a 0.05 significance level (alpha(α)=0.05)
up to 48 weeks.
|
Up to 48 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean change in ACS guideline score at 24 weeks
Time Frame: Up to 24 weeks
|
The ACS Guideline Score is comprised of scores on participant reported food intake (score range from 0-2), physical activity (score range from 0-2), and body mass index (BMI) (score range from 0-2).
The total score is calculated by summing the scores on each component with a total score range from 0 to 6. Greater scores indicate a greater level of healthy choices made by the participant.
The investigator will assess the independent and interaction effects of the four treatment components on change in ACS score as repeated measures and using a generalized linear mixed effect model, starting with the saturated model, including coefficients for main effects, interactions up to 3-way, and stratification variables (gender and age), and reduce the model via backward variable selection with a 0.05 significance level (α=0.05) up to 24 weeks.
|
Up to 24 weeks
|
|
Mean change in scores on the individual components of the ACS at 24 weeks
Time Frame: Up to 24 weeks
|
The ACS Guideline Score is comprised of individual factor scores on (1) participant reported food intake (score range from 0-2), (2) physical activity (score range from 0-2), and (3) body mass index (BMI) (score range from 0-2).
Greater scores indicate a greater level of healthy choices made by the participant.
The investigator will assess the independent and interaction effects of the four treatment components on change in the individual ACS guideline factors from 0 to 24 weeks using linear mixed-effects models adjusting for the stratification variables gender and age with the individual factor of interest as the outcome.
|
Up to 24 weeks
|
|
Mean change in scores on the individual components of the ACS at 48 weeks
Time Frame: Up to 48 weeks
|
The ACS Guideline Score is comprised of individual factor scores on (1) participant reported food intake (score range from 0-2), (2) physical activity (score range from 0-2), and (3) body mass index (BMI) (score range from 0-2).
Greater scores indicate a greater level of healthy choices made by the participant.
The investigator will assess the independent and interaction effects of the four treatment components on change in the individual ACS guideline factors from 0 to 48 weeks using linear mixed-effects models adjusting for the stratification variables gender and age with the individual factor of interest as the outcome.
|
Up to 48 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Erin Van Blarigan, ScD, University of California, San Francisco
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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)
October 21, 2021
Primary Completion (Estimated)
April 30, 2027
Study Completion (Estimated)
April 30, 2027
Study Registration Dates
First Submitted
September 14, 2021
First Submitted That Met QC Criteria
September 14, 2021
First Posted (Actual)
September 24, 2021
Study Record Updates
Last Update Posted (Actual)
June 2, 2026
Last Update Submitted That Met QC Criteria
May 29, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Urogenital Diseases
- Genital Diseases
- Endocrine System Diseases
- Genital Neoplasms, Male
- Urogenital Neoplasms
- Neoplasms by Site
- Neoplasms
- Genital Diseases, Male
- Prostatic Diseases
- Male Urogenital Diseases
- Kidney Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Intestinal Diseases
- Neoplasms by Histologic Type
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Digestive System Diseases
- Gastrointestinal Diseases
- Colorectal Neoplasms
- Intestinal Neoplasms
- Rectal Diseases
- Uterine Diseases
- Genital Diseases, Female
- Endocrine Gland Neoplasms
- Neoplasms, Glandular and Epithelial
- Adenocarcinoma
- Colonic Diseases
- Ovarian Diseases
- Adnexal Diseases
- Genital Neoplasms, Female
- Gonadal Disorders
- Skin Diseases
- Breast Diseases
- Urologic Neoplasms
- Carcinoma
- Uterine Neoplasms
- Urinary Bladder Diseases
- Skin and Connective Tissue Diseases
- Prostatic Neoplasms
- Rectal Neoplasms
- Colonic Neoplasms
- Ovarian Neoplasms
- Breast Neoplasms
- Carcinoma, Renal Cell
- Urinary Bladder Neoplasms
- Endometrial Neoplasms
- Kidney Neoplasms
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Health Services
- Health Care Facilities Workforce and Services
- Child Health Services
- Community Health Services
- Preventive Health Services
- Socioeconomic Factors
- Population Characteristics
- Behavioral Disciplines and Activities
- Mental Health Services
- Health Education
- Methods
- Early Intervention, Educational
- Educational Status
- Surveys and Questionnaires
- Health Promotion
- Counseling
Other Study ID Numbers
- 21456
- NCI-2021-09059 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- R37CA248774 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
De-identified data will be shared with research collaborators during the course of the study.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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