Insomnia Interventions in Cancer Survivors
This study looks at two different interventions used for the treatment of insomnia in survivors of breast, colon, lung, prostate and gynecologic cancer.
Ask AI to explain this studyKey things to know
This describes the study’s primary purpose.
The study team can explain what participation involves.
These are broad labels—not an eligibility decision.
Checked against the public recordLast updated May 26, 2016 · Source: ClinicalTrials.gov
Ask the study team to confirm whether enrollment is open.
Interventional
Locations may change over time.
Study sponsor
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- The Cooper Health System
- Interventions being studied
- Behavioral: CBT; Behavioral: MBSR
How this study is categorized
These labels come from structured fields and exact terms in the public record.
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.
- signed informed consent
- age 18 and over
- diagnosis of breast, colon, lung, prostate or gynecologic cancer that is non metastatic
- receiving treatment at one of the outpatient offices of the MD Anderson Cancer Center at Cooper
- Self reported insomnia
- Not currently taking any medications to treat insomnia
- No medical or psychological condition that would prevent successful protocol completion in the opinion of investigator.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- MD Anderson Cancer Center at CooperCamden, New Jersey
- MD Anderson Cancer Center at CooperVoorhees Township, New Jersey
Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 26, 2016. Always confirm current availability with the study team.