Skip to main content
OpenTrials
Completed

NCT Number: NCT05203614

Positive Activities for Asian American Cancer Patients and Caregivers

Positive Activities for Asian American Cancer Patients and Caregivers

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

M D Anderson Cancer Center

Houston, Texas, 77030, United States

About this study

Primary Objectives:

The overall objective of this project is to design and test the feasibility of two positive activities, household contribution and outside contribution, to increase quality of life in AA cancer patients.

Secondary Objectives:

Aim 1: To assess the acceptability and feasibility of household and outside contribution positive activities for AAs through a mixed qualitative and exploratory quantitative investigation.

Aim 2: To use the qualitative and quantitative data from Aim 1, in collaboration with the mentorship team, AA community members, and clinicians, to develop one or both positive activity intervention(s) (i.e., household or outside contribution) specifically for AA cancer patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for patients will be:

  • self-identifies as AA,
  • males or females ages 25-75 years
  • within 1 year of any cancer diagnosis
  • actively undergoing systemic therapy (e.g., chemotherapy, radiation)
  • able to identify a caregiver (e.g., spouse) who lives in the same household and consents to participate in the study,
  • able to read, write, and speak English (i.e., English proficient; EP),
  • access to internet, computer/phone, and web browser.

Exclusion criteria

for patients will be:

  • life expectancy less than 6 months in the opinion of the primary physician,
  • inability to stand or walk on their own or other physical limitations that preclude them from participating (3+ on ECOG performance status),
  • major thought disorder (e.g., schizophrenia or bipolar [patient records or

Inclusion criteria

for caregivers will be:

  • identifies as AA,
  • patient considers them to be caregiver, -
  • EP,
  • access to computer/phone, internet, and web browser.

Exclusion criteria

for caregivers will be:

  • unwilling or unable to participate in the study for any reason,
  • under the age of 18.

Treatment and study plan

Household Contribution

Behavioral

Questionnaires

Outside Contribution

Behavioral

Questionnaires

Control

Behavioral

Questionnaires

Primary outcomes

  1. Quality of Life Questionnaires(HRQOL & interpersonal well-being )

    Time frame: through study completion, an average of 1 year

    Hedonic well-being (positive and negative emotions) will be measured using a modified 12-item Affect-Adjective Scale (AAS)42 that includes low-arousal emotion items (e.g., peaceful/serene, dull/bored).

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Collaborators

  • National Institutes of Health (NIH)

Registry information

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Jan 24, 2022
Registry last updated
Nov 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.