Remote Psychosocial Intervention for Brain Tumour Survivors
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|ClinicalTrials.gov Identifier: NCT02439931|
Recruitment Status : Unknown
Verified May 2015 by British Columbia Cancer Agency.
Recruitment status was: Not yet recruiting
First Posted : May 12, 2015
Last Update Posted : May 13, 2015
|Condition or disease||Intervention/treatment||Phase|
|Quality of Life||Behavioral: Remote psychosocial intervention||Not Applicable|
Show Detailed Description
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||10 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Feasibility Study of a Remote Psychosocial Intervention for Brain Tumour Survivors|
|Study Start Date :||July 2015|
|Estimated Primary Completion Date :||July 2016|
|Estimated Study Completion Date :||September 2016|
Experimental: Remote psychosocial intervention
10 sessions of remotely delivered psychoeducation and support
Behavioral: Remote psychosocial intervention
- Change from baseline in score on Quality of Life score on the Functional Assessment of Cancer Therapy-Brain [ Time Frame: Comparison of scores pre-intervention to immediately post intervention (10 weeks) and 4 month followup ]The Functional Assessment of Cancer Therapy-Brain (FACT-Br) is a self report measure designed to assess quality of life in people living with brain malignancy across five dimensions: physical well-being, social/family well-being, emotional well being, functional well-being, and disease specific challenges.
- Changes in scores regarding psychological distress(anxiety, depression and somatization) on the Brief Symptom Inventory -18 [ Time Frame: Comparison of scores pre-intervention to immediately post intervention (10 weeks) and 4 month followup ]The Brief Symptom Inventory -18 is a commonly used self report measure of psychological distress in oncology patients.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02439931
|Contact: Douglas P Ozier, PhD.||604-877-6000 ext firstname.lastname@example.org|
|Principal Investigator:||Douglas P Ozier, PhD||British Columbia Cancer Agency|