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Mindfulness Based Stress Reduction: Supportive Treatment for Adult Patients With Cancer and Their Partners

Mindfulness Based Stress Reduction: Supportive Treatment for Adult Patients With Cancer and Their Partners

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01074528
Enrollment
150
Registered
2010-02-24
Start date
2010-04-30
Completion date
2017-05-31
Last updated
2017-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

cancer patients, relatives or partners of cancer patients

Brief summary

The main purpose of this study is to evaluate the effects of the Mindfulness Based Stress Reduction (MBSR) training program that is offered in the investigator hospital, more specifically on quality of life, coping strategies and partner relationship by using questionnaires. To asses the possible impact of this treatment on the latter domain, partners of the patients with a cancer diagnosis are invited to join the training program.

Detailed description

Patients with breast cancer often experience anxiety, depression, stress and reduced quality of life. As such, there is an increased interest in the implementation of the Mindfulness-Based Stress Reduction program as an additional supportive treatment. MBSR is a structured group program that aims at reducing stress levels by enhancing awareness of the present moment in combination with a non-judgemental attitude. The study evaluates the effects of an 8-week MBSR program on quality of life, mood, depression, stress and coping skills in breast cancer patients. Breast cancer patients of the Breast Clinic of the Universitair Ziekenhuis Brussel participate in the MBSR program. Before and after the training program patients filled out questionnaires evaluating quality of life, coping skills, emotional functioning, stress and aspects of mindfulness.

Interventions

8-week mindfulness training program

Sponsors

Belgian Federal Public Service, Food Chain Safety and Environment
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

For patients: * Cancer diagnosis * Between the age of 18 until 70 * Dutch speaking For partners: * between the age of 18 until 70 * dutch speaking

Exclusion criteria

for patients and partners: * Ongoing radiation therapy * Psychiatric disorders * Previous experience with mindfulness or meditation related techniques * Pregnancy * No or insufficient understanding of the Dutch language

Design outcomes

Primary

MeasureTime frame
quality of life (FACT) before trainingday 1
Quality of life (FACT) after trainingday 48

Secondary

MeasureTime frame
Perceived Stress Scale (PSS)day 1
Freiburg Mindfulness Scaleday 1
Cancer Coping Questionnaire (CCQ)day 1
Freiburg Mindfulness Inventory (FMI)day48
Profile of Mood Scale (POMS)day 48
Profile Of Mood Scale (POMS)day 1

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026