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Clinical Trials/NCT01783418
NCT01783418
Completed
Not Applicable

A Randomized, Wait-list Controlled Clinical Trial: the Effects of a Mindfulness-based Intervention on Quality of Life, Sleep and Mood in Adolescents With Cancer.

St. Justine's Hospital1 site in 1 country15 target enrollmentAugust 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pediatric Cancer
Sponsor
St. Justine's Hospital
Enrollment
15
Locations
1
Primary Endpoint
Changes in Mood From Baseline to Post-intervention and 6 Months Post-intervention
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effects of a mindfulness-based meditation intervention on quality of life, sleep and mood in adolescents with cancer compared to a control group.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
September 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
St. Justine's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Catherine Malboeuf-Hurtubise

Ph.D. Candidate, clinical psychology, Université de Montréal

St. Justine's Hospital

Eligibility Criteria

Inclusion Criteria

  • Teenagers (ages 12-18) with cancer

Exclusion Criteria

  • No ongoing or lifetime severe psychopathology, such as schizophrenia, psychosis, delusional disorders or organic mental disorders

Outcomes

Primary Outcomes

Changes in Mood From Baseline to Post-intervention and 6 Months Post-intervention

Time Frame: Baseline, Post-intervention (8 weeks)

PANAS-C - Negative affect Score range: 0 (minimum score) - 50 (maximum score) Higher scores represent worse outcomes

Changes in Quality of Life From Baseline to Post-intervention and 6 Months Post-intervention

Time Frame: Baseline, Post-intervention (8 weeks)

Pediatric Cancer Quality of Life Inventory Scale range: 0 (minimum score) to 108 (maximum score) Higher scores represent better outcomes

Changes Sleep From Baseline to Post-intervention and 6 Months Post-intervention

Time Frame: Baseline, Post-intervention (8 weeks)

Pittsburgh Sleep Quality Index Score range: 0 (minimum score) - 21 (maximum score) Higher scores indicate worse outcomes

Secondary Outcomes

  • Changes in Mindfulness Propensity and Skills From Baseline to Post-intervention and 6 Months Post-intervention(Baseline, Post-intervention (8 weeks))

Study Sites (1)

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