Neoplasms

Blood and Lymph Conditions

All Conditions

Skin and Connective Tissue Diseases

Gland and Hormone Related Diseases

Immune System Diseases

Digestive System Diseases

Rare Diseases

Leukemia

Carcinoma

Breast Neoplasms

Melanoma

Thyroid Neoplasms

Thyroid Diseases

Sarcoma

Lymphoma

Melanoma, Cutaneous Malignant

Colorectal Neoplasms

Skin Neoplasms

Breast Diseases

Skin Diseases

Intestinal Neoplasms

Gastrointestinal Neoplasms

Digestive System Neoplasms

Gastrointestinal Diseases

Colonic Diseases

Intestinal Diseases

Rectal Diseases

Neuroendocrine Tumors

Neuroectodermal Tumors

Neuroectodermal Tumors, Primitive

Neoplasms, Germ Cell and Embryonal

Neoplasms by Histologic Type

Neoplasms, Nerve Tissue

Nevus, Pigmented

Nevus

Nevi and Melanomas

Endocrine Gland Neoplasms

Head and Neck Neoplasms

Endocrine System Diseases

Soft Tissue Sarcoma

Lymphosarcoma

Neuroendocrine Tumor

Neuroepithelioma

Patients receive a personalized SCP and use the INSPIRE mobile application. Patients may receive telehealth stepped care after 1 month.

Patients receive access to a study-specific control website that has annotated links to existing resources for AYA survivors. After 12 months, patients receive a personalized SCP and have access to the digital INSPIRE intervention program without telehealth calls.

Internet Mobile Technology

Access to a study-specific control website

Internet-Based Intervention

Questionnaire Administration

Supportive Care

Informational Intervention

Study Intake

Patricia A. Ganz

Ann H. Partridge

Danielle N. Friedman

Linda Jacobs

K. Scott Baker

This trial studies how well an interactive survivorship program works in improving healthcare resources in adolescent and young adult cancer survivors. By improving access to survivorship resources, health literacy, self-management skills, and support, an interactive survivorship program may help to improve adherence to adolescent and young adult healthcare guidelines and reduce cancer-related distress.

OUTLINE: Patients who have one or more elevated distress or low cardiometabolic or cancer health care adherence are randomized to Arm I or II.

ARM I (INTERVENTION): Patients receive a personalized Survivorship Care Plan (SCP) and use the Interactive Survivorship Program to Improve Healthcare Resources (INSPIRE) mobile application. Patients may receive telehealth stepped care after 1 month.

ARM II (CONTROL): Patients receive access to a study-specific control website that has annotated links to existing resources for adolescent and young adult (AYA) survivors. After 12 months, patients receive a personalized SCP and have access to the digital INSPIRE intervention program without telehealth calls.

Interactive Survivorship Program for the Improvement of Healthcare Resources in Adolescent and Young Adult Cancer Survivors, INSPIRE-AYA Study

INSPIRE-AYA: A Multicenter Interactive Survivorship Program to Improve Healthcare Resources for Adolescent and Young Adult (AYA) Cancer Survivors

Will be assessed by Cancer and Treatment Distress (CTXD). The CTXD is a 22 item Likert type scale that contains 6 subscales: uncertainty, health burden, identity, medical demands, finances, and family strain. Scores on individual items range from 0 (none) to 3 (severe) distress related to an aspect of the cancer experience. Patients will meet the primary endpoint for lack of distress if they score \< 0.9 on the CTXD.

Patients will meet each HCA endpoint if their percent of recommended screenings obtained within the past 12 months is \>= 80% for HCA-CM.

Patients will meet each HCA endpoint if their percent of recommended screenings obtained within the past 12 months is \>= 80% for HCA-SM.

Patients will meet HCA endpoint if their percent of recommended screenings obtained within the past 12 months is \>= 80% for HCA-all.

National Cancer Institute (NCI)

Fred Hutchinson Cancer Center

AIM I: Participants follow an individually tailored gradual reduction of smoking schedule for 5 weeks while MDACC eHealth adapts WebCASSI into a smartphone app: Quitting Schedule.

AIM II: Participants pre-test the Quitting Schedule mobile smartphone app for 5 weeks.

Use Quitting Schedule mobile smartphone app

Interview

Participate in individual smoking cessation program

Smoking Cessation Intervention

Paul Cinciripini

This trial studies how well a mobile smartphone application called Quitting Schedule works in helping participants to quit smoking. Quitting Schedule is based on WebCASSI, a computer-based initiative that offered state of-the-art smoking cessation treatment and counseling to MD Anderson Cancer Center (MDACC) patients and served as a portal for non-patients to find information regarding smoking cessation advice and treatments. Quitting Schedule may help participants to quit smoking.

PRIMARY OBJECTIVES:

I. To adapt the internal algorithms of the scheduled reduced smoking approach in Computer Assisted Stop Smoking Intervention for the World Wide Web (WebCASSI) into a smartphone application (app): Quitting Schedule.

II. Once the smartphone app is developed, a pretesting phase with smoker seeking care at MDACC Tobacco Treatment Program or another community service such as Equality Texas, Lesbian, Gay, Bisexual, Transgender, and Queer (LGBTQ) Advisory Board of the City of Houston, Montrose Center, Avenue 360 and Lesbian Health Initiative will follow.

III. To culturally and linguistically adapt Quitting Schedule app into Spanish language.

IV. To implement a feasibility trial in IDC (Colombia), INCan (Mexico), and INEN (Peru).

OUTLINE:

AIM I: Participants follow an individually tailored gradual reduction of smoking schedule for 5 weeks while MDACC eHealth adapts WebCASSI into a smartphone app: Quitting Schedule.

AIM II: Participants pre-test the Quitting Schedule mobile smartphone app for 5 weeks.

Quitting Schedule Mobile Smartphone Application in Helping Participants to Quit Smoking

Project Quitting Schedule

A focus group will be used in order to provide feedback on the features of the app in relation to usability for smoking cessation and future app development.

M.D. Anderson Cancer Center

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Interactive Survivorship Program for the Improvement of Healthcare Resources in Adolescent and Young Adult Cancer Survivors, INSPIRE-AYA Study	NCT04593277	Clinical Stage ... Clinical Stage ... Clinical Stage ... Hematopoietic a... Invasive Malign... Leukemia Lymphoma Malignant Solid... Sarcoma Stage I Colorec... Stage II Colore... Stage III Color... Anatomic Stage ... Anatomic Stage ... Anatomic Stage ... Thyroid Gland C...	Internet Mobile... Internet-Based ... Questionnaire A... Supportive Care Informational I...	18 Years -	Fred Hutchinson Cancer Center
Quitting Schedule Mobile Smartphone Application in Helping Participants to Quit Smoking	NCT03668769	Cigarette Smoke... Current Every D... Current Smoker Malignant Neopl...	Internet Mobile... Interview Questionnaire A... Smoking Cessati...	18 Years -	M.D. Anderson Cancer Center

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