TCU: Taking Care of Us: A Dyadic Intervention for Heart Failure Couples

Sponsor
Boston College (Other)
Overall Status
Recruiting
CT.gov ID
NCT04737759
Collaborator
National Institute on Aging (NIA) (NIH)
144
2
2
16.8
72
4.3

Study Details

Study Description

Brief Summary

This research study is evaluating the efficacy and feasibility of a novel, dyadic intervention for heart failure couples versus an educational counseling intervention.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Taking Care of Us
  • Other: SUPPORT
N/A

Detailed Description

There is a critical need for theoretically- and empirically-driven dyadic interventions to improve the outcomes of both adults with heart failure and their partners. The proposed study will evaluate a novel, dyadic program, Taking Care of Us, versus an educational counseling condition using a randomized controlled trial on 72 couples living with heart failure. Both programs are offered via Zoom by trained interventionists and last approximately two months.

Specifically, we will 1) determine the efficacy of the Taking Care of Us intervention on dyadic health; 2) determine the efficacy of the Taking Care of Us intervention on dyadic appraisal and dyadic management; and 3) determine the feasibility and acceptability of the Taking Care of Us intervention.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
144 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Taking Care of Us: A Dyadic Intervention for Heart Failure
Actual Study Start Date :
Jul 9, 2021
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Taking Care of Us

Taking Care of Us involves seven sessions delivered via Zoom to couples over approximately two months. Sessions last approximately 45-60 minutes and are delivered by a trained interventionist. The program is a communication-based, relationship-focused intervention that is strengths-based and fosters new skills to support couples managing heart failure. The goals of the program are to 1) target the couple with heart failure as a team; 2) increase shared appraisal within the couple; 3) improve communication skills within the couple; 4) improve collaboration within the couple and dyadic management of heart failure; 5) improve confidence within the couple; and 6) improve both individual and dyadic health and well-being.

Behavioral: Taking Care of Us
A social-behavioral intervention that is targeted at the couple living with heart failure and delivered via Zoom.

Active Comparator: SUPPORT

The SUPPORT program involves three sessions delivered via Zoom to couples over approximately two months. Sessions last approximately 45-60 minutes and are delivered by a trained interventionist. This arm is an educational intervention to support management of heart failure.

Other: SUPPORT
SUPPORT is an educational counseling intervention that is targeted at the couple living with heart failure and delivered by Zoom.

Outcome Measures

Primary Outcome Measures

  1. Change in quality of life scores in couples in the TCU vs SUPPORT condition assessed by the 10-item PROMIS Global Health Short Form measure [5 months after baseline]

    PROMIS Global Health Short Form measures physical, mental and overall quality of life. Higher scores indicate better quality of life

Secondary Outcome Measures

  1. Change in depressive symptom scores in couples in the TCU vs SUPPORT condition as assessed by the 20-item Center for Epidemiological Studies Depression CESD measure. [5 months after baseline]

    Center for Epidemiological Studies Depression CESD measure. Lower scores indicate fewer depressive symptoms.

  2. Change in healthcare utilization scores in couples in the TCU vs SUPPORT condition as assessed by the 5-item Stanford Patient Education Research Center PERC Healthcare Utilization measure. [5 months after baseline]

    Stanford PERC Healthcare Utilization measure collects physician, mental health, emergency room visits and hospitalizations. Lower scores indicate less healthcare utilization.

  3. Change in care strain scores in spouses in the TCU vs SUPPORT condition as assessed by the 16-item Multidimensional Caregiver Strain Index. [5 months after baseline]

    Multidimensional Caregiver Strain Index measures physical, social, interpersonal strain and time constraints and demands related to providing care. Lower scores indicate less strain.

  4. Change in heart failure related quality of life scores in persons with heart failure in the TCU vs SUPPORT condition as assessed by the 12-item Kansas City Cardiomyopathy Questionnaire. [5 months after baseline]

    Kansas City Cardiomyopathy Questionnaire. Higher scores indicate better heart failure related quality of life.

  5. Change in difference in dyspnea scores in couples in the TCU vs SUPPORT condition as assessed by the 6-item Heart Failure Somatic Perception Scale. [5 months after baseline]

    Difference in scores is measured by comparing the scores of both the person with heart failure and their spouse. Scores closer to zero indicate less difference.

  6. Change in difference in pain interference scores in couples in the TCU vs SUPPORT condition as assessed by the 6-item PROMIS Pain Interference measure. [5 months after baseline]

    Difference in scores is measured by comparing the scores of both the person with heart failure and their spouse. Scores closer to zero indicate less difference.

  7. Change in difference in fatigue scores in couples in the TCU vs SUPPORT condition as assessed by the 8-item PROMIS Fatigue measure. [5 months baseline]

    Difference in scores is measured by comparing the scores of both the person with heart failure and their spouse. Scores closer to zero indicate less difference.

  8. Change in collaboration scores in couples in the TCU vs SUPPORT condition as assessed by the 6-item Collaboration in Chronic Illness measure. [5 months after baseline]

    Collaboration in Chronic Illness measure. Higher scores indicate greater collaboration within couples.

  9. Change in confidence scores in couples in the TCU vs SUPPORT condition as assessed by the 6-item Stanford Confidence to Manage Chronic Illness measure. [5 months after baseline]

    Stanford Confidence to Manage Chronic Illness measure. Higher scores indicate greater confidence.

  10. Change in communication scores in couples in the TCU vs SUPPORT condition as assessed by the 11-item Dyadic Coping Scale. [5 months after baseline]

    Dyadic Coping Scale. Higher scores indicate greater communication (both active communication and less protective buffering)

Other Outcome Measures

  1. Change in satisfaction scores in couples in the TCU vs SUPPORT condition as assessed by the Satisfaction and Advantages/Drawbacks measure. [5 months after baseline]

    Satisfaction and Advantages/Drawbacks measure. Higher scores indicate greater satisfaction with assigned program.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria: Adults with Heart Failure:
  • Diagnosis of heart failure for at least three months

  • Current heart failure symptoms (i.e., NYHA Class II-III; AHA/ACC Stage C)

  • Age greater than or equal to 18 years

  • Willing and able to provide informed consent

  • Reachable by telephone/email

  • Access to device with camera (e.g., computer, tablet) to participate in Zoom sessions

  • Have a co-residing spouse/unmarried partner willing to participate

Inclusion Criteria: Spouses/Partners:
  • Age greater than or equal to 18 years

  • Co-residing with the adult with heart failure at time of recruitment

  • Have lived with the adult with heart failure for at least one year

  • Willing and able to provide informed consent

Exclusion Criteria:
  • Major and uncorrected hearing impairment

  • Significant cognitive impairment

  • Heart transplantation/mechanical circulatory support prior to enrollment

  • Concomitant terminal illness that would impede participation

  • Active psychosis or severe substance abuse that would impair the ability to complete the study

  • Inability to complete the requirements of the study, including enrolment in an additional trial

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tufts Medical Center Boston Massachusetts United States 02111
2 Boston College Chestnut Hill Massachusetts United States 02467

Sponsors and Collaborators

  • Boston College
  • National Institute on Aging (NIA)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Karen Lyons, Associate Professor, Boston College
ClinicalTrials.gov Identifier:
NCT04737759
Other Study ID Numbers:
  • 21.074
  • R21AG068715
First Posted:
Feb 4, 2021
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Karen Lyons, Associate Professor, Boston College
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2022