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Piloting GETCare: A Remote Goal-based Education and Skills Training Program for Caregivers Poststroke

Piloting GETCare: A Remote Goal-based Education and Skills Training Program for Caregivers Poststroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05403021
Acronym
GETCare
Enrollment
28
Registered
2022-06-02
Start date
2020-08-31
Completion date
2021-08-20
Last updated
2022-06-02

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

Conditions

Stroke

Keywords

caregiver, intervention, pilot, education, goals, skills

Brief summary

The purpose of this study was to evaluate the GETCare program, a Goal-based Education and skills Training program for Caregivers poststroke.

Detailed description

The purpose of this study was to utilize a single-arm mixed method pilot trial to evaluate the5-week GETCare program with the following study aims: (1) explore feasibility and acceptability, (2) assess knowledge acquisition and goal attainment, and (3) test preliminary effects on key caregiver outcomes. This remote program included guided goal setting, individualized resource recommendations, and education modules.

Interventions

BEHAVIORALGETCare Intervention

This 5-week intervention was administered remotely and individually to caregivers utilizing phone, email, and a secure online platform. The GETCare program was mostly self-led and included five weekly module education topics: basics of stroke, caregiver skills, caregiver changes, meaningful participation, and community resources. Each module incorporated (1) individualized education, (2) goal setting, (3) skills training, and (4) community resource recommendations. The program was led by a licensed occupational therapist who is a certified stroke rehabilitation specialist. The occupational therapist conducted weekly check-ins via email or phone focused on answering questions, tracking goal progress, and assisting in problem solving.

Sponsors

Utah Occupational Therapy Association
CollaboratorUNKNOWN
University of Utah
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

single-arm mixed method pilot trial

Eligibility

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

Inclusion criteria

* self-identification as a primary caregiver (direct care involvement) of someone who had a stroke (no restriction on stroke duration) * ≥ 18 years old * access to internet/telephone throughout the study * able to speak, read, and understand English * person with stroke expected to discharge within 1 month if still in the hospital

Exclusion criteria

* unable to read and follow basic instructions * indicated the individual with stroke had no deficits poststroke

Design outcomes

Primary

MeasureTime frameDescription
Revised Scale for Caregiving Self-efficacyBaselineScores range 0-100, higher score indicates higher self-efficacy
Perceived Stress ScaleBaselineScores range 0-40, higher score indicates higher perceived stress

Secondary

MeasureTime frameDescription
Patient-Reported Outcomes Measurement Information System-43 Profile v2.1Baseline43 items across seven domains: physical function, anxiety, fatigue, depression, sleep disturbance, ability to participate in social roles and activities, and pain interference; Scores range 6-30 for each subscale. For subscales of anxiety, depression, fatigue, and sleep disturbance, higher scores indicate worse symptoms. For subscale of social participation, higher scores indicate improved symptoms. Subscales of physical function and pain interference were not included in analyses, since they were not expected to change through this intervention.
Neuro-Quality of Life (Neuro-QOL) Positive Affect and Well-being v1.0Baseline9 items; Scores range 9-45, higher score indicates higher positive affect and well-being
Knowledge assessmentBaselineEvaluate knowledge acquisition of weekly education topics; Scores range 0-35, higher score indicates higher knowledge
Canadian Occupational Performance MeasureBaselineAssesses importance of goal, current performance of goal, and satisfaction with current performance of goal; Scores range 0-10, higher score indicates higher importance, performance, and satisfaction with performance
Neuro-Quality of Life (Neuro-QOL) Positive Affect and Well-beingPost-intervention (approximately 6 weeks)9 items; Scores range 9-45, higher score indicates higher positive affect and well-being
Modified Caregiver Strain IndexBaselineScores range 0-26, higher score indicates higher caregiver strain

Other

MeasureTime frameDescription
Feedback surveyPost-intervention (approximately 6 weeks)Included a variety of questions (no/yes, Likert scales, and open-ended questions) regarding feedback of the intervention. For example, Please indicate how helpful the additional handouts and videos were for you (0 = not at all helpful, 1 = a little helpful, 2 = somewhat helpful, 3 = quite helpful, 4 = extremely helpful).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026