SmartCare: Innovations in Caregiving Interventions (SmartCare)

August 28, 2017 updated by: Paula Sherwood, University of Pittsburgh
This is a study to evaluate the effectiveness of using an established intervention for depressive symptom management in conjunction with a needs-based caregiver intervention for improving the psychological and physical health of family caregivers of persons recently diagnosed with a Primary Malignant Brain Tumor.

Study Overview

Detailed Description

We have designed a needs-based intervention to improve neuro-oncology caregivers' health. Our novel approach treats depressive symptoms prior to implementing a needs-based intervention in a sample of PMBT family caregivers who score above threshold on depressive symptoms. Study outcomes are psychological responses (unmet needs, depressive symptoms, anxiety, and burden) and physical responses (levels of stimulated and circulating IL-6 and IL-1β, C-reactive protein, peripheral blood mono-nuclear cells, physical symptoms, and new diagnoses or exacerbations of co-morbid conditions). The proposed study addresses research priorities set by both NCI and NINR to improve the quality of life of patients and their families and NINR's emphasis on integrating bio-behavioral science and adopting, adapting and generating new technologies.

Primary aims:

  1. Compare the efficacy of a) an intervention for depressive symptoms (Beating the Blues) delivered prior to a needs-based caregiver intervention (SmartCare©) versus b) SmartCare© alone versus c) enhanced care as usual (CAU+) in improving caregivers' psychological and physical responses.

    H1: At 4- and 6-months, caregivers who receive Beating the Blues prior to SmartCare© will display improved psychological and physical responses compared to caregivers who receive CAU+.

    H2: At 4- and 6-months, caregivers who receive SmartCare© alone will display improved psychological and physical responses compared to caregivers who receive CAU+.

    H3: At 4- and 6-months, caregivers who receive Beating the Blues prior to SmartCare© will display improved psychological and physical responses compared to those who receive SmartCare© alone.

  2. Compare the efficacy of Beating the Blues versus CAU+ in improving subjects' short-term psychological and physical responses.

H1: At 2-months following baseline, caregivers who receive Beating the Blues will display improved psychological and physical responses compared to CAU+.

Exploratory aims:

  1. Determine whether any changes in psychological and physical health resulting from receiving Beating the Blues prior to SmartCare© or SmartCare© alone are maintained at 10-months after baseline.
  2. Evaluate whether the effect of Beating the Blues + SmartCare© (vs. SmartCare© alone) on 4- and 6-month psychological and physical responses is mediated by 0- to 2-month changes in depressive symptoms.

Study Type

Interventional

Enrollment (Actual)

240

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Pittsburgh, Pennsylvania, United States, 15261
        • University of Pittsburgh, School of Nursing

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Care recipient:

  • Over 21 years of age.
  • Newly (within 1 month) diagnosed with a PMBT (tumor verified via pathology report to be a glioblastoma multiforme, anaplastic astrocytoma, anaplastic oligodendroglioma, anaplastic oligoastrocytoma, medulloblastoma, or anaplastic ependymoma).

Caregiver:

  • Primary nonprofessional, non-paid caregiver, as identified by the care recipient.
  • Over 21 years of age with telephone access.
  • Reads-speaks English
  • Obtains a score of >6 on the shortened CES-D.
  • Caregivers may or may not be receiving pharmacotherapy for depressive symptoms

Exclusion Criteria:

Caregiver:

  • Currently considers self to be a primary caregiver for anyone else other than children
  • Currently receiving any type of formal counselling for depressive symptoms

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: CAU+ (Enhanced Care as Usual)
CAU+ (Enhanced Care as Usual) is defined as the care received from the care recipient's oncologist supplemented by unlimited access to three components of the study website: caregiver guides, links to web-based resources, and a basic friends and family page for the 10 month duration of the study.
CAU+ is defined as the care received from the care recipient's oncologist supplemented by unlimited access to three components of the study website: caregiver guides, links to web-based resources, and a basic friends and family page. These resources are routinely available on the Internet. We provide these as a "one-stop shopping" resource in order to standardize care as usual for caregivers. All caregivers will be sent personalized e-mails from the project director every week during the intervention period.
Experimental: CAU+ and SmartCare
CAU+ (Enhanced Care as Usual) for eight weeks, followed by eight weeks of SmartCare. SmartCare is a web-based, nurse guided intervention for caregivers based on the Representational Approach of symptom management.
CAU+ is defined as the care received from the care recipient's oncologist supplemented by unlimited access to three components of the study website: caregiver guides, links to web-based resources, and a basic friends and family page. These resources are routinely available on the Internet. We provide these as a "one-stop shopping" resource in order to standardize care as usual for caregivers. All caregivers will be sent personalized e-mails from the project director every week during the intervention period.
SmartCare is a web-based, nurse guided intervention for caregivers based on the Representational Approach of symptom management. The RA builds on traditional cognitive-behavioral interventions by promoting in depth reflection of previous and current experiences, beliefs, and knowledge (referred to as representations) prior to providing new information or engaging in problem-solving.
Experimental: CAU+ and Beating the Blues and SmartCare
CAU+ (Enhanced Care as Usual) and Beating the Blues concurrently for eight weeks, followed by SmartCare for eight weeks. Beating the Blues is an established, web-based, self-directed, cognitive behavioral therapy for managing depressive symptoms.
CAU+ is defined as the care received from the care recipient's oncologist supplemented by unlimited access to three components of the study website: caregiver guides, links to web-based resources, and a basic friends and family page. These resources are routinely available on the Internet. We provide these as a "one-stop shopping" resource in order to standardize care as usual for caregivers. All caregivers will be sent personalized e-mails from the project director every week during the intervention period.
SmartCare is a web-based, nurse guided intervention for caregivers based on the Representational Approach of symptom management. The RA builds on traditional cognitive-behavioral interventions by promoting in depth reflection of previous and current experiences, beliefs, and knowledge (referred to as representations) prior to providing new information or engaging in problem-solving.
Beating the Blues is an established, self-directed, web-based cognitive behavioral therapy program for managing depressive symptoms. Caregivers are asked to complete 8 weekly sessions, each lasting approximately 50 minutes. Participants are also given simple "homework" after each lesson.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in depression from baseline at 4 months on the shortened CES-D
Time Frame: Baseline and 4 months
Depressive symptoms will be measured using the 10-item shortened version of the Center for Epidemiologic Studies - Depression (CES-D).
Baseline and 4 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in unmet needs from baseline at 4 months on the CNS
Time Frame: Baseline and 4 months
Unmet Needs will be measured via the Caregiver Needs Screen (CNS) questionnaire.
Baseline and 4 months
Change in mastery from baseline at 4 months on the Caregiver Mastery Scale
Time Frame: Baseline and 4 months
Mastery will be measured using the Caregiver Mastery Scale.
Baseline and 4 months
Change in optimism from baseline at 4 months on the Life Orientation Test
Time Frame: Baseline and 4 months
Optimism will be measured using the Life Orientation Test.
Baseline and 4 months
Change spirituality from baseline at 4 months on the FACIT.
Time Frame: Baseline and 4 months.
Spirituality will measured using the Functional Assessment of Chronic Illness Therapy - Sp (FACIT).
Baseline and 4 months.
Change in oversight demand from baseline at 4 months on the caregiver vigilance scale.
Time Frame: Baseline and 4 months
Caregiver oversight demand will be measured using the four item Caregiver Vigilance Scale.
Baseline and 4 months
Change in social support from baseline at 4 months on the ISEL.
Time Frame: Baseline and 4 months.
Social support will be measured using the Interpersonal Support Evaluation List (ISEL). Subjects rate the availability of three types of social support (appraisal, belonging, and tangible).
Baseline and 4 months.
Change in occupational functioning from baseline at 4 months on the WLQ.
Time Frame: Baseline and 4 months.
Caregiver occupational functioning will be measured by general questions related to employment status and the Work Limitations Questionnaire (WLQ).
Baseline and 4 months.
Changes in positive aspects of providing care from baseline at 4 months on the PAC.
Time Frame: Baseline and 4 months
Positive aspects of providing care will be measured using the Positive Aspects of Caregiving (PAC) scale.
Baseline and 4 months
Change in unmet needs from baseline at 6 months on the CNS
Time Frame: Baseline and 6 months
Unmet Needs will be measured via the Caregiver Needs Screen (CNS) questionnaire.
Baseline and 6 months
Change in mastery from baseline at 6 months on the Caregiver Mastery Scale
Time Frame: Baseline and 6 months
Mastery will be measured using the Caregiver Mastery Scale.
Baseline and 6 months
Change in optimism from baseline at 6 months on the Life Orientation Test
Time Frame: Baseline and 6 months
Optimism will be measured using the Life Orientation Test.
Baseline and 6 months
Change spirituality from baseline at 6 months on the FACIT.
Time Frame: Baseline and 6 months.
Spirituality will measured using the Functional Assessment of Chronic Illness Therapy - Sp (FACIT).
Baseline and 6 months.
Change in oversight demand from baseline at 6 months on the caregiver vigilance scale.
Time Frame: Baseline and 6 months
Caregiver oversight demand will be measured using the four item Caregiver Vigilance Scale.
Baseline and 6 months
Change in social support from baseline at 6 months on the ISEL.
Time Frame: Baseline and 6 months.
Social support will be measured using the Interpersonal Support Evaluation List (ISEL). Subjects rate the availability of three types of social support (appraisal, belonging, and tangible).
Baseline and 6 months.
Change in occupational functioning from baseline at 6 months on the WLQ.
Time Frame: Baseline and 6 months.
Caregiver occupational functioning will be measured by general questions related to employment status and the Work Limitations Questionnaire (WLQ).
Baseline and 6 months.
Changes in positive aspects of providing care from baseline at 6 months on the PAC.
Time Frame: Baseline and 6 months
Positive aspects of providing care will be measured using the Positive Aspects of Caregiving (PAC) scale.
Baseline and 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Paula R Sherwood, PhD, University of Pittsburgh, School of Nursing
  • Principal Investigator: Heidi S Donovan, PhD, University of Pittsburgh, School of Nursing

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2014

Primary Completion (Actual)

June 14, 2017

Study Completion (Actual)

June 14, 2017

Study Registration Dates

First Submitted

November 19, 2013

First Submitted That Met QC Criteria

February 6, 2014

First Posted (Estimate)

February 10, 2014

Study Record Updates

Last Update Posted (Actual)

August 29, 2017

Last Update Submitted That Met QC Criteria

August 28, 2017

Last Verified

August 1, 2017

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Non-identifiable data will be shared with interested parties in agreement with University policy.

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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