CompletedNot applicableNCT04885439
Official study title

NextSteps Intervention for Advanced Cancer Patients and Caregivers

Study summary

This study seeks to test the efficacy of a psychosocial intervention to empower advanced cancer patients and their caregivers and improve their quality of life (QOL). The program, called NextSTEPS, provides skills training in six domains that are central to patient and caregiver QOL: self-care, stress management, symptom management, effective communication, problem-solving, and social support.

Ask AI to explain this study
Start here

Key things to know

Main goalSupportive Care

This describes the study’s primary purpose.

What is being studiedNextSteps

The study team can explain what participation involves.

Who it may be forLung Cancer · Gastrointestinal Cancer

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Apr 22, 2024 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Baylor College of Medicine

Study sponsor

01
Study overview

What this study is about

Purpose
Supportive Care
Study type
Interventional
Phase
Not applicable
Sponsor
Baylor College of Medicine
Interventions being studied
Behavioral: NextSteps
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

1. Patient has stage 3A, 3B, or 4 NSLC or extensive stage SCLC and is within one month of treatment initiation OR patient has Stage 4 GI cancer and is within one month of treatment initiation 2. patient is spending more than 50% of time out of bed on a daily basis as measured by an ECOG Performance Status rating of level 0, 1, or 2 3. patient has stable brain metastases and no limitation on hepatic or renal function 4. patient has a spouse/partner other or close family member who he/she defines as the primary caregiver 5. patient and caregiver are age 18 years or older 6. patient and caregiver have the ability to read and understand English at a sixth grade level, as determined by ability to understand the consent form 7. patient and caregiver can provide informed consent

Reasons someone may not be able to joinExclusion criteria

1. patient or caregiver is deaf or has significant hearing impairment and thus cannot use the telephone 2. patient is currently enrolled in hospice.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Baylor College of MedicineHouston, Texas

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Apr 22, 2024. Always confirm current availability with the study team.

View original record ↗