Mindfulness Based Couples Therapy

NCT02349217 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2022-08-24

No results posted yet for this study

Summary

The goal of this study is to explore the effects of a Mindfulness Based Couples Intervention on relationship satisfaction with quality of life and immune system function among breast cancer survivors and their partners.

Conditions

Interventions

BEHAVIORAL

Mindfulness-Based Relationship Enhancement (MBRE)

Participant and partner take part in an 8-week Mindfulness-Based Relationship Enhancement (MBRE) intervention course. MBRE course consists of meditation and yoga techniques and handouts.

BEHAVIORAL

Self-Help Materials

Participants and partner receive self-help materials.

BEHAVIORAL

Pain Assessment

Pain assessment administered at baseline and at follow up visit. Pain assessment involves submerging hand in cold water.

BEHAVIORAL

Questionnaires

Questionnaires completed at baseline and at follow up visit. Questionnaires ask about fatigue, mood, stress, social support, marital satisfaction, depression, and general demographics (age, race and so on). It should take about 1½ hours total to complete the questionnaires.

BEHAVIORAL

Neurocognitive Tests

Neurocognitive tests administered at baseline and at follow up visit. Tests to check memory and thinking abilities.

PROCEDURE

Cortisol Tests

Cortisol testing performed after baseline visit and at follow up visit. Participants asked to collect saliva samples for cortisol assays immediately, 30, 45, and 60 minutes after awakening (representing the cortisol awakening response) and at noon, 4 P.M. and 8 P.M.

BEHAVIORAL

Interviews

Interviews conducted after follow up visit. These interviews are audio-taped and transcribed.

Sponsors & Collaborators

  • M.D. Anderson Cancer Center

    lead OTHER

Principal Investigators

  • Robert Dantzer, PHD · M.D. Anderson Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-23
Primary Completion
2022-08-01
Completion
2022-08-01

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02349217 on ClinicalTrials.gov