Depression and Anxiety Trial, Recruiting

Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

For healthcare professionals and researchers (Aim 1):

• People who have been personally invited by a member of the study team
• People working in healthcare (such as doctors, nurses, or pharmacists), patient advocacy, healthcare or technology research, or healthcare administration and management
• People aged 18 or older
• People who speak English
• People who are willing and able to give their informed consent to participate

For older cancer survivors living in rural areas (Aim 2):

• People who live in a rural area, as defined by the Health Resources & Services Administration (HRSA) rural classification system
• People who report having been diagnosed with any type of cancer
• People who report having finished their main cancer treatment (such as surgery, chemotherapy, targeted therapy, or hormone therapy) aimed at curing the cancer
• People who have access to a computer, smartphone, or tablet
• People aged 65 or older
• People whose screening results show a Cancer and Treatment Distress (CTXD) score above 0.85 (the trial site will assess this)
• People who have a caregiver who is willing to take part in the study
• People who are not living in an institution (such as a nursing home or care facility)
• People who are sufficiently proficient in English to participate
• People who are willing and able to give their informed consent to participate

For caregivers (Aim 2):

• People who are an informal caregiver (such as a partner, child, or friend) of an eligible rural older cancer survivor participating in this trial — caregivers may live in a rural or urban area and do not need to live with the cancer survivor
• People who have access to the internet
• People aged 18 or older
• People who are not living in an institution
• People who are sufficiently proficient in English to participate
• People who are willing and able to give their informed consent to participate

For the final workshop (Aim 3):

• People working as healthcare providers, medical or practice managers, patient care coordinators, or medical health technologists

Who may not be able to join:

For older cancer survivors living in rural areas (Aim 2):

• People whose cancer comes back, or who receive a new cancer diagnosis, while they are participating in the trial
• People who are currently admitted as inpatients in a hospital or medical facility
• People whose cognitive (thinking or memory) difficulties would prevent them from being able to give written informed consent

For caregivers (Aim 2):

• People who are currently admitted as inpatients in a hospital or medical facility
• People whose cognitive (thinking or memory) difficulties would prevent them from being able to give written informed consent

Important: Always verify eligibility with the trial site directly before applying.