CI

At a glance

ClinicalIndex Comparison Record
N/AWithdrawn· 0 enrolled
Drug / intervention
Residential Program +4 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02429544
NCT02429544N/AWithdrawn
Withdrawn

Effects of a Group Residential Retreat on Cancer Outcomes

M.D. Anderson Cancer Center·interventional·Posted Apr 29, 2015·Updated Aug 1, 2016

In Brief

A clinical study evaluating Residential Program, Questionnaires, and 3 other interventions for Breast Cancer. Withdrawn before enrollment.

Signals

Trial was withdrawn before enrollment

Detailed Summary

The goal of this behavioral research study is to compare 2 different types of residential group programs to help researchers learn if and how well these groups may help to improve physical and emotional well-being in patients with stage IV breast cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBreast Cancer
Countries--
Collaborators--

Timeline

N/AWithdrawnFinished
20162017201820192020202120222023202420252026
First PostedApr 29, 2015
Enrollment StartAug 1, 2016
Primary CompletionAug 1, 2018
TodayJul 1, 2026
Enrollment to primary: 2 yearsPosted 11.2 years ago

Interventions

Residential Programbehavioral

Participants attend a 7-day offsite, residential support program. On Day 5 of the program, participant joined by spouse or caregiver.

Questionnairesbehavioral

Questionnaires completed about mood, sleep, fatigue, how participant has been feeling, and their general quality of life at baseline visit, 1 month after baseline, 7 days after residential program ends, and again about 3 months later.

Electroencephalogram (EEG)device

EEG performed at baseline with simultaneous computer testing consisting of 3 tests to check attention, short-term memory, and levels of emotions. EEG repeated 7 days after the residential program ends, and then again about 3 months later.

Saliva Testingother

Day after baseline visit, saliva collected for 3 days at different times to measure cortisol levels. Saliva testing repeated 7 days after the residential program ends, and then again about 3 months later.

Study Diary plus Actigraphbehavioral

For seven days after baseline visit, participants complete study diary describing sleeping habits. An actigraph also worn during this time to record physical activity and sleeping habits.