UnknownNot applicableNCT02783079

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.

Checked against the public recordLast updated May 26, 2016 · Source: ClinicalTrials.gov

StatusUnknown
PhaseNot applicable
U.S. locations2
SponsorThe Cooper Health System
01
Study overview

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
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

Inclusion Criteria: * 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.

04
Study sites

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.

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