- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02792608
Mindfulness-Based Therapy for Brain Tumour Survivors
A Mindfulness-Based Intervention to Improve Quality of Life Among Brain Tumour Survivors
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Increased survival rates and life expectancy of primary BT survivors today have resulted in a need to expand the focus from acute treatment to reducing disability and long-term symptom burden in survivorship. Many BT survivors are left with reduced autonomy in their lives, with a lower likelihood of independent living and increased risk of functional and symptom adversity (pain and physical disability), unemployment, and family difficulties. Unsurprisingly, these factors are associated with increased stress, psychological suffering, and reduced QOL. Research has noted the prevalence of psychological distress and cognitive impairment, experienced as late effects, with up to 90% of survivors experiencing some form of cognitive impairment and depressive symptoms, as well as many as 80% experiencing mental fatigue and up to 60% experiencing anxiety.
80% of all central nervous system tumour survivors exhibit rehabilitation needs, and survivors report an interest in learning coping techniques for stress, yet the majority of symptoms remain underestimated and untreated. BT survivors are left with limited treatment options to promote long-term wellbeing, with 71% of resources containing minimal to no information on coping with outcomes. Despite considerable research demonstrating BT survivors increased risk of symptom burden and reduced QOL, there has been little research on treatment or effective interventions.
Some outpatient rehabilitation therapies have been made available to other neurologically impaired populations (e.g. Traumatic Brain Injury, Stroke) but evidence in support of specific approaches has been equivocal, with limited rehabilitative research in BT survivors specifically. Such treatments for the broader ABI population to-date have included Cognitive Behavioural Therapy (CBT) and Applied Behavioural Analysis (ABA), with debatable effectiveness. Positive studies have suggested that treatment may only prove effective for a handful of ABI sequelae. Studies to date are marred by limited methodological rigour and applicability to the BT population because of the broader, heterogeneous ABI focus. As a result, healthcare professionals and national organizations, such as National Coalition for Cancer Survivorship, have called for higher quality research to inform novel treatments to improve outcomes for specific groups, such as the BT population.
In response to these calls, Mindfulness-Based Therapy's (MBTs) have been proposed as a plausible treatment for long term care of ABI survivors, in general. MBTs use a non-stigmatizing approach, combining secularized eastern meditative practices with western psychological advances. MBTs have good evidence that they improve a wide range of sequelae, including, stress, depression, anxiety and cognitive impairment. MBT efficacy has been repeatedly demonstrated across multiple psychiatric, neurological, and cancer populations. MBTs focus on acceptance-based and adaptive approaches, which might theoretically be better suited to the realities of the lives of BT survivors, than would change-based approaches such as CBT or ABA. MBT participants learn to generate less distress, engage more positively in their lives, and respond to difficult situations more adaptively; they often describe it as transformative.
MBTs have begun to be studied in the broader ABI survivor population, and this emerging literature suggests efficacy in reducing symptom burden. However, there are no known studies considering the effectiveness of an MBT for BT survivors specifically; the present study aims to fill this important knowledge gap. The goal of this study is to test the effectiveness of a five session MBT course in reducing depressive symptoms and perceived stress, as well as improving overall QOL and wellbeing for BT survivors.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M4N 3M5
- Sunnybrook Health Sciences Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- consenting brain tumour survivor at The Odette Cancer Centre
- >six months post-treatment
- Ability to communicate, in written and spoken English
Exclusion Criteria:
- Minimal depressive symptoms (score below 14 on the BDI-II)
- Previous head injuries or non-BT neurological diseases
- Unaware of deficits (determined through clinical judgement)
- Substance abuse / dependence within three months
- History of dementia, a recent suicide attempt, or current self-injurious behavior
- Previously completed >four weeks of a MBI, or general CBT, in the past three years
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindfulness-based Therapy
5 week, manual-based group MBI treatment for depression
|
MBT will be delivered in group format, 135 minutes per week, for 5 consecutive weeks with 10-20 participants per group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline Depressive Symptoms at 5 Weeks
Time Frame: Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
Scale used to measure Depressive Symptoms: Beck Depression Inventory II (BDI-II)
|
Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline Quality of Life at 5 Weeks
Time Frame: Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
Scale used to measure Quality of Life: Quality of Life after Brain Injury (QOLBRI)
|
Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
|
Change from Baseline Perceived Stress at 5 Weeks
Time Frame: Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
Scale used to measure Perceived Stress: Perceived Stress Scale (PSS)
|
Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
|
Change from Baseline Mental Wellbeing at 5 Weeks
Time Frame: Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
Scale used to measure Mental Wellbeing: Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS)
|
Pre- (Week 0) and Post-Treatment Assessment (Week 5)
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Steven Selchen, MD MSt FRCPC, Sunnybrook Health Sciences Centre
- Principal Investigator: Janet Ellis, MB MD FRCPC, Sunnybrook Health Sciences Centre
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 169-2015
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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