No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
21 – 100
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
125 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Other
Who this trial is looking for
This trial is looking for Latino people with solid tumor cancer who are dealing with depression, trouble sleeping, and fatigue. Participants will try a special mental health support called DESCANSO, which can be done through telehealth.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 21 years old.
I live in mainland U.S. or Puerto Rico.
I identify as Latino/a or Hispanic.
Spanish is my preferred language.
I speak Spanish well.
I have a solid tumor cancer diagnosed at stages I, II, or III.
I am currently undergoing treatment or have finished treatment within the last year.
I experience fatigue and have trouble sleeping.
You may not be able to join if
I have cognitive impairment that prevents me from giving informed consent.
I have a history of conditions in the past year that affect fatigue and sleep, like sleep apnea or drug abuse.
I am pregnant or breastfeeding.
I feel suicidal.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The purpose of this study is to improve ways of providing mental health support to Spanish-speaking Latino participants who have cancer and experience depression, insomnia, and fatigue. Investigators will test a special mental health intervention called DESCANSO/REST (Depresión/Depressed Mood, Cansancio/Fatigue, and Sueño/Sleep). The intervention can be delivered through telehealth.
Trial Locations
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Eligibility Criteria
Provider Eligibility Criteria:
Participant eligibility will be determined by a self-report screener. Inclusion Criteria Self-Report Criteria
* Mental health provider
* Treats Latino cancer patients and/or survivors
* Has at least 3 years of clinical experience providing psychosocial services to ca…
Provider Eligibility Criteria:
Participant eligibility will be determined by a self-report screener. Inclusion Criteria Self-Report Criteria
* Mental health provider
* Treats Latino cancer patients and/or survivors
* Has at least 3 years of clinical experience providing psychosocial services to cancer patients and/or survivors
* Able to read Spanish determined by the question: "Can you read in Spanish? Yes/No"
Patient Eligibility Criteria:
A patient cannot be considered eligible for this study unless ALL of the following conditions are met. Participant eligibility will be determined by an initial EMR review followed by a self-report screener.
Inclusion Criteria EMR Criteria
* Documentation of Disease
o Pathologically confirmed solid tumor cancer (either most recent or new diagnosis)
* Definition of Disease \[or Measurable Disease\]
o Diagnosed with stages I, II, or III
* Prior Treatment
* Currently undergoing systemic therapy (chemotherapy, radiation therapy, and/or immunotherapy) or within the first year following completion of systemic therapy Self-Report Criteria
* Age ≥ 21 years
* Lives in mainland U.S. or Puerto Rico
* Identifies as Latino/a or Hispanic
* Reports Spanish as their preferred language
* Speaks Spanish "Very well" or "Well" as determined by the question: "How well do you speak Spanish?"
* Presence of fatigue and disturbed sleep determined by a score of ≥ 3 on the MD Anderson Symptom Inventory
Exclusion Criteria EMR Criteria
o In the judgment of the treating physician, protocol investigators, and/or study staff, presence of cognitive impairment (e.g., delirium or dementia) sufficient to preclude meaningful informed consent and/or study participation
Self-Report Criteria
* History of comorbidities within the last 12 months associated with fatigue and poor sleep, including hypothyroidism or abnormal thyroid function, sleep apnea, chronic obstructive pulmonary disease, neuromuscular disease, alcohol or drug abuse
* Pregnant or lactating, women only
* Presence of suicidal risk determined by any affirmative response on the Columbia-Suicide Severity Rating Scale
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