Mindfulness Clinical Trial
Official title:
The Effects of Resourcefulness Training Intervention and Decentering on Self-Management of Stress in Caregivers of Children With Complex Chronic Conditions Dependent on Lifesaving Medical Technology: A Pilot Study
Verified date | September 2019 |
Source | University Hospitals Cleveland Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators will conduct a randomized clinical trial pilot study to examine the
effectiveness of a theoretically based intervention (called ReMind) encompassing two key
components: (a) Resourcefulness Training for parent caregivers, and (b) daily mindfulness
meditation delivered using a smart phone application (Stop, Breathe & Thinkā¢) with an
intervention (Mind Only) that consists only of daily mindfulness meditation. Both components
of the intervention have been tested separately (but not combined) and both interventions can
be self-tailored, which meets the vital need for these caregivers to engage in
self-management activities when it is convenient for them. The investigators will test the
two arms of the intervention in 30 parents of technology-dependent children, 15 parents in
each group. The investigators will collect mixed data at baseline, 3 months and 6 months
after subject enrollment to describe changes in proximal and distal outcomes. The
investigators aim to:
1. Evaluate the intermediate (3 month) and long-term (6 month) effects of the ReMind and
Mind Only interventions on study mediators (HPA Axis Function and stress, cognitive
factors, resourcefulness) and determine if there are different effects between ReMind
and Mind Only interventions.
2. Evaluate the differences in distal psychological (Mental Health Related Quality of Life,
Depressive Cognitions, Depressive Symptoms, Anxiety, Caregiver Burden), physical
(Physical Health Related Quality of Life), and cost outcomes between subjects in the
ReMind and Mind Only arms over time.
3. Determine the moderating effects of parents' social support, demographics (age, gender,
family income) and children's functional status on (a) proximal outcomes and the
relationship between (a) the intervention arm and distal outcomes, and (b) HPA Axis
Function, stress, cognitive factors and distal outcomes.
4. Evaluate the impact of decentering on the association between the interventions and the
proximal and distal outcomes.
5. Explore differences in neurological processing (DMN and TPN) and decentering in proximal
and distal outcomes associated with each intervention.
Status | Completed |
Enrollment | 31 |
Est. completion date | March 30, 2019 |
Est. primary completion date | March 30, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. parent (biological, adoptive, or foster mother, father, grandmother, or grandfather) caregiver for a child aged =17 years dependent on medical technology (mechanical ventilators, intravenous nutrition/medication, respiratory or nutritional support) at home; 2. aged =18 years; 3. able to speak and understand English. Exclusion Criteria: 1. currently practicing mindfulness-based interventions (yoga, meditation, deep breathing) 2 history of a medical condition or procedure that is contraindicated for imaging (i.e. cardiac pacemaker, sternal wires, or metal implants); 3 claustrophobia requiring anxiolytics or sedation 4 Pregnancy at time of recruitment. 5 If participant becomes pregnant during the follow up period the participant will be excluded from all imaging studies. |
Country | Name | City | State |
---|---|---|---|
United States | University Hospitals Cleveland Medical Center | Cleveland | Ohio |
Lead Sponsor | Collaborator |
---|---|
University Hospitals Cleveland Medical Center | Case Western Reserve University, The Cleveland Clinic |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline Mental & Physical Health Related Quality of Life at 3 Months & 6 Months | Measure using the Patient Reported Outcomes Measurement Information System (PROMIS)-29 | Measured at baseline with follow up at 3 months, 6 months | |
Secondary | Change from Baseline Appraised Sleep Quality at 3 months and 6 months | Measure using Pittsburgh Sleep Quality Index | Measured at baseline with follow up at 3 months, 6 months | |
Secondary | Change from Baseline Positive Health Practices at 3 months and 6 months | Measure using Personal Lifestyle Questionnaire | Measured at baseline with follow up at 3 months, 6 months |
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