Behavioral Activation for Post-Stroke Sedentary Behavior Using Telehealth

Stroke Clinical Trial

— teleABLE  

Official title:

teleABLE: Adapting a Behavioral Activation-Based Intervention to Reduce Post-Stroke Sedentary Behavior Using Telehealth (Formative Phase)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05029284
• Other study ID #: 2021-0059
• Secondary ID: K23HL159240
• Status: Completed
• Phase: N/A
• Start date: December 20, 2021
• Est. completion date: March 18, 2024

Study information

• Verified date: April 2024
• Source: University of Minnesota
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Adults with stroke-related disability spend more time sedentary than adults without stroke-related disability, which places them at risk for poor cardiovascular health outcomes. Few interventions are designed to reduce post-stroke sedentary time.

The purpose of this research is to test whether the teleABLE (Activating Behavior for Lasting Engagement) Intervention is feasible and acceptable to adults within the first 12 months post-stroke. The hypothesis is that teleABLE can be feasibly delivered using videoconferencing within the first 12 months post-stroke. 10 participants will complete assessments and activity monitoring (activPAL micro3) at 0 (baseline) and 8 (post-intervention)-weeks. Participants will complete 12 sessions of the teleABLE intervention.

Findings from this study will be used to guide the intervention protocol in the planned next phase of this research.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: March 18, 2024
• Est. primary completion date: March 18, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Stroke diagnosis =12 months prior to study enrollment

• =6 hours of sedentary behavior on a typical weekday (assessed by Sedentary Behavior Questionnaire)

• Ambulatory with or without assistive device (assessed by Functional Independence Measure, mobility score =5)

• Able to access an electronic device (smartphone, tablet, or computer) that is compatible with a videoconferencing application

• Able to identify a support person with whom the participant has face-to-face interaction at least one time per week

• Able and willing to participate fully in the study and provide informed consent

Exclusion Criteria:

• Currently receiving care in an inpatient rehabilitation, transitional care unit, or skilled nursing facility

• Severe cognitive or communication impairments (inability to respond accurately to complete study telephone screening or complete informed consent)

• Comorbid neurodegenerative disorder (e.g. Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis, myasthenia gravis, dementia, Alzheimer's disease, Huntington's disease, glioblastoma)

• Comorbid cancer, currently undergoing chemotherapy or radiation treatment

• Comorbid major depressive disorder (assessed by Patient Health Questionnaire-2, score =2)

• Received inpatient treatment or hospitalized for psychiatric condition and/or alcohol or substance abuse within the past 12 months

• Diagnosis of a terminal illness and/or in hospice care

• History of skin sensitivity that precludes the use of medical tape necessary for adherence to activity monitor measure

• Inability to speak, read, or understand English

• Concurrent participation in another rehabilitation intervention research study

• Investigator discretion for safety or adherence reasons

Related Conditions & MeSH terms

• Hemorrhagic Stroke
• Ischemic Stroke
• Stroke
• Stroke Hemorrhagic
• Stroke, Ischemic

Intervention

Behavioral:
• teleABLE
Participants will be guided to self-monitor their daily activities, schedule personally meaningful non-sedentary activities, collaboratively problem solve to overcome barriers to the activity, and self-assess their progress. Participants may be asked to self-monitor their activity levels and complete planned activities between sessions.

Locations

Country	Name	City	State
United States	University of Minnesota	Minneapolis	Minnesota

Sponsors (2)

Lead Sponsor	Collaborator
University of Minnesota	National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Treatment-Emergent Adverse Events	The count of treatment-related serious (e.g. injurious) and non-serious (e.g. fall without injury) adverse events that occur during intervention delivery will be reported.	week 2 through week 7
Primary	Participant Satisfaction	Assessed by the Client Satisfaction Questionnaire-8. This is an 8-item questionnaire with each item ranked on an 1 to 4 Likert-type scale. We will compute the mean score across all items. The possible range is 1 to 4, with high scores indicating high satisfaction.	week 8
Secondary	Change in Participation Restrictions	Assessed by the Activity Card Sort 3. This is a 100-item tool during which participants indicate whether they did the activity prior to their stroke, continue to do the activity since their stroke, or have given up the activity since their stroke. Change in the proportion of activities retained will be reported.	week 0 to week 8
Secondary	Change in Health-Related Quality of Life	Assessed by the EuroQol-5 Dimension-5 Level. This is a 5-item self-report questionnaire with each item scored on a 1 to 5 scale. Scores are converted to Index Scores following published procedures (possible range -0.573 to 1), with high scores indicating high quality of life.	week 0 to week 8
Secondary	Change in Sedentary Minutes	Assessed using the activPAL micro3 monitor following a 7-day wear protocol. The mean daily minutes of sitting time accumulated in bouts of 30 minutes or more will be computed for each time point. Change in mean daily minutes of sitting time accumulated in bouts of 30 minutes or more will be reported.	week 0 to week 8