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Connect-Home Clinical Trial

Connect-Home: Testing the Efficacy of Transitional Care of Patients and Caregivers During Transitions From Skilled Nursing Facilities to Home

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03810534
Enrollment
654
Registered
2019-01-18
Start date
2019-03-01
Completion date
2021-09-12
Last updated
2022-08-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Caregivers, Frailty, Patient Discharge, Transitional Care

Keywords

Transitional Care, Skilled Nursing Facilities

Brief summary

This study will test whether transitional care targeting care needs of seriously ill, skilled nursing facility (SNF) patients and their caregivers will help to improve SNF patient outcomes (preparedness for discharge, quality of life, function and acute care use) and caregiver outcomes (preparedness for the caregiving role. caregiver burden and caregiver distress).

Detailed description

Prior research has not established an evidence-based model of transitional care for seriously ill SNF patients (and their caregivers) who transfer from SNF to home-based care. Connect-Home, the intervention to be tested in this study, will use existing nursing home staff and community-based nurses to deliver transitional care in SNFs and the patient's home. The feasibility, acceptability, and estimated efficacy of Connect-Home was demonstrated in a pilot test of pre-discharge elements of Connect-Home (N=133 patients and their caregivers). Compared to controls, intervention participants were significantly more prepared for discharge (higher scores on Care Transitions Measure-15) and they more frequently received individualized plans for continuing care at home. Virtually all SNF staff participants (97%) recommended the intervention for future use, demonstrating its acceptability. The objective of this study is to test the efficacy of Connect-Home for seriously ill patients discharged to home and their caregivers. In this trial, intervention participants will receive the Connect-Home intervention; the intervention has two steps. While the patient is in the SNF, nurses, social workers and rehabilitation therapists will create an individualized Transition Plan of Care and prepare the patient and caregiver to manage the patient's serious illness at home. Within 24 hours of the time that the SNF patient discharges to home, a Connect-Home Activation Nurse (Activation RN) will visit the patient at home; the Activation RN will help the patient and family caregiver implement the written Transition Plan of Care. The Connect-Home intervention will focus on six key care needs: (1) home safety and level of assistance; (2) advance care planning; (3) symptom management; (4) medication reconciliation; (5) function and activity; and (6) coordination of follow-up medical care. In this trial, the control participants will receive usual discharge planning in the SNF only. Usual discharge planning for SNF patients includes assignment to an interdisciplinary team that develops discharge instructions for the patient to follow at home with oversight by a physician. Usual care does not include a structured home visit after the patient discharges to home. Patient and caregiver outcomes will assessed in 7, 30, and 60 days after the patient discharged from the SNF to home. Outcomes assessors will be blinded to study group.

Interventions

BEHAVIORALConnect-Home

Connect-Home will introduce organizational structure to support delivery of transitional care processes. New elements of structure include:electronic health record (EHR) template, Connect-Home Toolkit, and Staff Training. After structural elements are added, SNF staff will use Connect-Home care processes to deliver the 2-step transitional care intervention.In Step 1, SNF nurses, therapists, and social workers will develop a Transition Plan of Care and prepare the patient and caregiver to manage the patient's serious illness and functional needs. In Step 2, the Connect-Home Activation RN will visit the patient's home within 24 hours of discharge; the nurse will activate the Transition Plan of Care at home. Both intervention steps focus on 6 key care needs to optimize patient and caregiver outcomes: 1) home safety and level of assistance; 2) advance care planning; 3) symptom management; 4) medication reconciliation; 5) function and activity; and 6) coordination of follow-up medical care.

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

The Connect-Home study employs a stepped wedge cluster-randomized trial design, which is a crossover design at the cluster level where clusters of individuals (i.e., residents in a nursing home) crossover from control to intervention condition at randomly assigned timepoints or steps.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

for patients: * English-speaking * Have a Minimum Data Set 3.0 Section GG Mobility Assessment Score of 3 or less, indicating the patient requires at least 25-50% assistance for functional mobility * Be diagnosed with at least 1 serious medical illness (neurodegenerative dementia, cancer, chronic kidney disease, cirrhosis, congestive heart failure, chronic obstructive or interstitial lung disease, acute infection with sepsis, acute major motor stroke, acute coronary syndrome, acute hip fracture, diabetes with end organ complications, or intensive care for \>3 days while hospitalized) * Having a caregiver who can be enrolled in the study * For patients with cognitive impairment additional criteria include documentation in the medical record of a caregiver who is the patient's legally authorized representative; and consent of the caregiver to participate in the study as the patient's representative. Inclusion Criteria for Caregivers: * English-speaking * Self-reports assisting the patient at home.

Exclusion criteria

for Patients: * Planned hospital readmission for procedures/treatments in next 90 days. There are no

Design outcomes

Primary

MeasureTime frameDescription
Care Transitions Measure-15 Score 7 Days After Skilled Nursing Facility Discharge7 Days After SNF DischargeThe patient's preparedness for discharge will be measured by the Care Transitions Measure-15 (CTM-15), which includes 5 items on a 4-point scale. The CTM-15 measures self-reported knowledge and skills for continuing care at home. Summary score range 0-100, with higher scores associated with less acute care use after discharge.
Preparedness for Caregiving Scale Score 7 Days After Patient's Skill Nursing Facility Discharge7 Days After Patient SNF DischargeThe caregiver's preparedness for caregiving will be measured by the Preparedness for Caregiving Scale (PCS), which includes 8 items on a five-point Likert scale (0-4). The PCS measures self-reported readiness for caregiving. Range = 0-32, with higher scores associated with less anxiety.

Secondary

MeasureTime frameDescription
Life Space Assessment 30 Days After Skilled Nursing Facility Discharge30 Days After SNF DischargePatient's function will be measured using the Life Space Assessment, which includes 5 Likert scales corresponding to a hierarchy of levels of mobility (each scored from 0-4) where weights are the product of the Life-space level (range 1-5) and the independence score (range 1-2). The range is 1-120. Lower scores are associated with falls and hospitalization.
Life Space Assessment 60 Days After Skilled Nursing Facility Discharge60 Days After SNF DischargePatient's function will be measured using the Life Space Assessment, which includes 5 Likert scales corresponding to a hierarchy of levels of mobility (each scored from 0-4) where weights are the product of the Life-space level (range 1-5) and the independence score (range 1-2). The range is 1-120. Lower scores are associated with falls and hospitalization.
Zarit Caregiver Burden Scale 30 Days After Skilled Nursing Facility Discharge30 Days After Patient's SNF DischargeCaregiver burden will be measured using the Zarit Caregiver Burden Scale, which includes 12 items on a five-point scale, measuring caregiver perceptions that caregiving has an adverse effect on their emotional, social, financial, physical and spiritual functioning. Scores range 0-48; higher scores are associated with depression and social isolation.
Zarit Caregiver Burden Scale 60 Days After Skilled Nursing Facility Discharge60 Days After Patient's SNF DischargeCaregiver burden will be measured using the Zarit Caregiver Burden Scale, which includes 12 items on a five-point scale, measuring caregiver perceptions that caregiving has an adverse effect on their emotional, social, financial, physical and spiritual functioning. Scores range 0-48; higher scores are associated with depression and social isolation.
McGill Quality of Life Questionnaire-Revised Score 30 Days After Skilled Nursing Facility Discharge30 Days After SNF DischargeThe patient's quality of life will be measured using the McGill Quality of Life Questionnaire-Revised (MQoL-R), which includes 14 items on a ten-point Likert scale. The scale is recommended for studies of palliative care and measures quality of life across disease trajectories. Range = 0-10, with higher score indicating better quality of life. There are 4 MQOL-R subscales. Each subscale score is the mean of its items that range from 0-10. The Total Score, also ranging from 0-10, is the mean of the subscale score means.
Distress Thermometer 60 Days After Skilled Nursing Facility Discharge60 Days After Patient's SNF DischargeCaregiver distress will be measured using the Distress Thermometer, which includes 1 item on an 11-point scale, measuring negative affect (e.g., sadness and fear) related to caregiving for a severely ill person. Score ranges 0-10, with scores \>4 associated with poor coping and depression.
Self-Reported Days of ED or Hospital Use 30 Days After Skilled Nursing Facility Discharge30 Days After SNF DischargePatient's days of acute care use will be measured using the self-reported number of combined number of days the patient spends in the Emergency Department (ED) or hospital in 30 days after SNF discharge.
Self-Reported Days of ED or Hospital Use 60 Days After Skilled Nursing Facility Discharge60 Days After SNF DischargePatient's days of acute care use will be measured using the self-reported number of combined number of days the patient spends in the ED or hospital in 60 days after SNF discharge.
Distress Thermometer 30 Days After Skilled Nursing Facility Discharge30 Days After Patient's SNF DischargeCaregiver distress will be measured using the Distress Thermometer, which includes 1 item on an 11-point scale, measuring negative affect (e.g., sadness and fear) related to caregiving for a severely ill person. Score ranges 0-10, with scores \>4 associated with poor coping and depression.
McGill Quality of Life Questionnaire-Revised Score 60 Days After Skilled Nursing Facility Discharge60 Days After SNF DischargeThe patient's quality of life will be measured using the McGill Quality of Life Questionnaire-Revised (MQoL-R), which includes 14 items on a ten-point Likert scale. The scale is recommended for studies of palliative care and measures quality of life across disease trajectories. Range = 0-10, with higher score indicating better quality of life. There are 4 MQOL-R subscales. Each subscale score is the mean of its items that range from 0-10. The Total Score, also ranging from 0-10, is the mean of the subscale score means.

Countries

United States

Participant flow

Participants by arm

ArmCount
Connect-Home Patients
Connect-Home intervention at the skilled nursing facility and at the subject's home. Participants will have data collected at 7, 30, and 60 days post SNF discharge.
165
Connect-Home Caregivers
Caregivers of Connect-Home study patients.
165
Control Patients
Standard discharge planning at the skilled nursing facility only. Participants will have data collected at 7, 30, and 60 days post SNF discharge.
162
Control Caregivers
Caregivers of Control study patients.
162
Total654

Baseline characteristics

CharacteristicConnect-Home PatientsTotalControl CaregiversControl PatientsConnect-Home Caregivers
Age, Continuous76.5 Years
STANDARD_DEVIATION 9.49
76.5 Years
STANDARD_DEVIATION 9.51
60.9 Years
STANDARD_DEVIATION 13.72
76.6 Years
STANDARD_DEVIATION 9.55
58.1 Years
STANDARD_DEVIATION 14.02
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
165 Participants654 Participants162 Participants162 Participants165 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
37 Participants157 Participants43 Participants40 Participants37 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
5 Participants25 Participants6 Participants3 Participants11 Participants
Race (NIH/OMB)
White
123 Participants472 Participants113 Participants119 Participants117 Participants
Region of Enrollment
United States
165 Participants654 Participants162 Participants162 Participants165 Participants
Sex: Female, Male
Female
104 Participants444 Participants116 Participants105 Participants119 Participants
Sex: Female, Male
Male
61 Participants210 Participants46 Participants57 Participants46 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
6 / 1650 / 1658 / 1620 / 162
other
Total, other adverse events
0 / 1650 / 1650 / 1620 / 162
serious
Total, serious adverse events
38 / 1650 / 16534 / 1620 / 162

Outcome results

Primary

Care Transitions Measure-15 Score 7 Days After Skilled Nursing Facility Discharge

The patient's preparedness for discharge will be measured by the Care Transitions Measure-15 (CTM-15), which includes 5 items on a 4-point scale. The CTM-15 measures self-reported knowledge and skills for continuing care at home. Summary score range 0-100, with higher scores associated with less acute care use after discharge.

Time frame: 7 Days After SNF Discharge

Population: Data reported for participants who answered the 7-day data collection phone call.

ArmMeasureValue (MEAN)Dispersion
Connect-HomeCare Transitions Measure-15 Score 7 Days After Skilled Nursing Facility Discharge75.80 score on a scaleStandard Deviation 16.08
ControlCare Transitions Measure-15 Score 7 Days After Skilled Nursing Facility Discharge68.33 score on a scaleStandard Deviation 17.69
p-value: 0.62Mixed Models Analysis
Primary

Preparedness for Caregiving Scale Score 7 Days After Patient's Skill Nursing Facility Discharge

The caregiver's preparedness for caregiving will be measured by the Preparedness for Caregiving Scale (PCS), which includes 8 items on a five-point Likert scale (0-4). The PCS measures self-reported readiness for caregiving. Range = 0-32, with higher scores associated with less anxiety.

Time frame: 7 Days After Patient SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomePreparedness for Caregiving Scale Score 7 Days After Patient's Skill Nursing Facility Discharge23.14 score on a scaleStandard Deviation 6.74
ControlPreparedness for Caregiving Scale Score 7 Days After Patient's Skill Nursing Facility Discharge19.26 score on a scaleStandard Deviation 6.42
p-value: 0.31Mixed Models Analysis
Secondary

Distress Thermometer 30 Days After Skilled Nursing Facility Discharge

Caregiver distress will be measured using the Distress Thermometer, which includes 1 item on an 11-point scale, measuring negative affect (e.g., sadness and fear) related to caregiving for a severely ill person. Score ranges 0-10, with scores \>4 associated with poor coping and depression.

Time frame: 30 Days After Patient's SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeDistress Thermometer 30 Days After Skilled Nursing Facility Discharge3.19 score on a scaleStandard Deviation 2.66
ControlDistress Thermometer 30 Days After Skilled Nursing Facility Discharge3.02 score on a scaleStandard Deviation 3.08
p-value: 0.48Mixed Models Analysis
Secondary

Distress Thermometer 60 Days After Skilled Nursing Facility Discharge

Caregiver distress will be measured using the Distress Thermometer, which includes 1 item on an 11-point scale, measuring negative affect (e.g., sadness and fear) related to caregiving for a severely ill person. Score ranges 0-10, with scores \>4 associated with poor coping and depression.

Time frame: 60 Days After Patient's SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeDistress Thermometer 60 Days After Skilled Nursing Facility Discharge3.03 score on a scaleStandard Deviation 3.07
ControlDistress Thermometer 60 Days After Skilled Nursing Facility Discharge2.60 score on a scaleStandard Deviation 2.73
p-value: 0.22Mixed Models Analysis
Secondary

Life Space Assessment 30 Days After Skilled Nursing Facility Discharge

Patient's function will be measured using the Life Space Assessment, which includes 5 Likert scales corresponding to a hierarchy of levels of mobility (each scored from 0-4) where weights are the product of the Life-space level (range 1-5) and the independence score (range 1-2). The range is 1-120. Lower scores are associated with falls and hospitalization.

Time frame: 30 Days After SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeLife Space Assessment 30 Days After Skilled Nursing Facility Discharge22.18 score on a scaleStandard Deviation 16.67
ControlLife Space Assessment 30 Days After Skilled Nursing Facility Discharge22.97 score on a scaleStandard Deviation 15.38
p-value: 0.53Mixed Models Analysis
Secondary

Life Space Assessment 60 Days After Skilled Nursing Facility Discharge

Patient's function will be measured using the Life Space Assessment, which includes 5 Likert scales corresponding to a hierarchy of levels of mobility (each scored from 0-4) where weights are the product of the Life-space level (range 1-5) and the independence score (range 1-2). The range is 1-120. Lower scores are associated with falls and hospitalization.

Time frame: 60 Days After SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeLife Space Assessment 60 Days After Skilled Nursing Facility Discharge25.55 score on a scaleStandard Deviation 17.41
ControlLife Space Assessment 60 Days After Skilled Nursing Facility Discharge28.60 score on a scaleStandard Deviation 18.55
p-value: 0.83Mixed Models Analysis
Secondary

McGill Quality of Life Questionnaire-Revised Score 30 Days After Skilled Nursing Facility Discharge

The patient's quality of life will be measured using the McGill Quality of Life Questionnaire-Revised (MQoL-R), which includes 14 items on a ten-point Likert scale. The scale is recommended for studies of palliative care and measures quality of life across disease trajectories. Range = 0-10, with higher score indicating better quality of life. There are 4 MQOL-R subscales. Each subscale score is the mean of its items that range from 0-10. The Total Score, also ranging from 0-10, is the mean of the subscale score means.

Time frame: 30 Days After SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeMcGill Quality of Life Questionnaire-Revised Score 30 Days After Skilled Nursing Facility Discharge7.69 score on a scaleStandard Deviation 1.81
ControlMcGill Quality of Life Questionnaire-Revised Score 30 Days After Skilled Nursing Facility Discharge7.69 score on a scaleStandard Deviation 1.79
p-value: 0.93Mixed Models Analysis
Secondary

McGill Quality of Life Questionnaire-Revised Score 60 Days After Skilled Nursing Facility Discharge

The patient's quality of life will be measured using the McGill Quality of Life Questionnaire-Revised (MQoL-R), which includes 14 items on a ten-point Likert scale. The scale is recommended for studies of palliative care and measures quality of life across disease trajectories. Range = 0-10, with higher score indicating better quality of life. There are 4 MQOL-R subscales. Each subscale score is the mean of its items that range from 0-10. The Total Score, also ranging from 0-10, is the mean of the subscale score means.

Time frame: 60 Days After SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeMcGill Quality of Life Questionnaire-Revised Score 60 Days After Skilled Nursing Facility Discharge7.81 score on a scaleStandard Deviation 1.58
ControlMcGill Quality of Life Questionnaire-Revised Score 60 Days After Skilled Nursing Facility Discharge7.71 score on a scaleStandard Deviation 1.73
p-value: 0.6Mixed Models Analysis
Secondary

Self-Reported Days of ED or Hospital Use 30 Days After Skilled Nursing Facility Discharge

Patient's days of acute care use will be measured using the self-reported number of combined number of days the patient spends in the Emergency Department (ED) or hospital in 30 days after SNF discharge.

Time frame: 30 Days After SNF Discharge

Population: Data are reported only for participants who had acute care use.

ArmMeasureValue (MEAN)Dispersion
Connect-HomeSelf-Reported Days of ED or Hospital Use 30 Days After Skilled Nursing Facility Discharge.65 DaysStandard Deviation 1.82
ControlSelf-Reported Days of ED or Hospital Use 30 Days After Skilled Nursing Facility Discharge1.01 DaysStandard Deviation 3.46
p-value: 0.88Mixed Models Analysis
Secondary

Self-Reported Days of ED or Hospital Use 60 Days After Skilled Nursing Facility Discharge

Patient's days of acute care use will be measured using the self-reported number of combined number of days the patient spends in the ED or hospital in 60 days after SNF discharge.

Time frame: 60 Days After SNF Discharge

Population: Data are reported only for participants who had acute care use.

ArmMeasureValue (MEAN)Dispersion
Connect-HomeSelf-Reported Days of ED or Hospital Use 60 Days After Skilled Nursing Facility Discharge.82 DaysStandard Error 2
ControlSelf-Reported Days of ED or Hospital Use 60 Days After Skilled Nursing Facility Discharge1.24 DaysStandard Error 3.61
p-value: 0.23Mixed Models Analysis
Secondary

Zarit Caregiver Burden Scale 30 Days After Skilled Nursing Facility Discharge

Caregiver burden will be measured using the Zarit Caregiver Burden Scale, which includes 12 items on a five-point scale, measuring caregiver perceptions that caregiving has an adverse effect on their emotional, social, financial, physical and spiritual functioning. Scores range 0-48; higher scores are associated with depression and social isolation.

Time frame: 30 Days After Patient's SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeZarit Caregiver Burden Scale 30 Days After Skilled Nursing Facility Discharge12.27 score on a scaleStandard Deviation 9.77
ControlZarit Caregiver Burden Scale 30 Days After Skilled Nursing Facility Discharge12.33 score on a scaleStandard Deviation 10.33
p-value: 0.75Mixed Models Analysis
Secondary

Zarit Caregiver Burden Scale 60 Days After Skilled Nursing Facility Discharge

Caregiver burden will be measured using the Zarit Caregiver Burden Scale, which includes 12 items on a five-point scale, measuring caregiver perceptions that caregiving has an adverse effect on their emotional, social, financial, physical and spiritual functioning. Scores range 0-48; higher scores are associated with depression and social isolation.

Time frame: 60 Days After Patient's SNF Discharge

ArmMeasureValue (MEAN)Dispersion
Connect-HomeZarit Caregiver Burden Scale 60 Days After Skilled Nursing Facility Discharge11.84 score on a scaleStandard Deviation 9.4
ControlZarit Caregiver Burden Scale 60 Days After Skilled Nursing Facility Discharge11.35 score on a scaleStandard Deviation 8.94
p-value: 0.5Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026