The goal of this clinical trial is to evaluate a program for adults who live alone and have some cognitive impairment (CI) to see if it is useful and acceptable. This program aims to help older adults with cognitive impairment who live alone to be engaged and active, as well as safe at home. The investigators want to see how useful this program is and how it can be improved. The specific aims are: * Specific Aim 1: Develop and Adapt Home Alone to Prepare for Pilot Testing. * Specific Aim 2: Pilot Test a Revised Version of Home Alone. Phase I participants will be asked to: * Participate for 3 months * Complete 3 surveys * Complete 7 1-hour meetings on a weekly basis with a coach * Complete a final interview Phase II participants will be asked to: * Participate for 6 months * Complete 3 surveys * Complete 7 1-hour meetings on a weekly basis with a coach * A sub-sample will be asked to complete a final interview
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Acceptability of Intervention
Timeframe: Phase I at 1 month
Acceptability of Intervention
Timeframe: Phase I at 3 months
Acceptability of Intervention
Timeframe: Phase II at 3 months
Acceptability of Intervention
Timeframe: Phase II at 6 months
Feasibility of Intervention
Timeframe: Phase I at 1 month
Feasibility of Intervention
Timeframe: Phase I at 3 months
Feasibility of Intervention
Timeframe: Phase II at 3 months
Feasibility of Intervention
Timeframe: Phase II at 6 months
Intervention Appropriateness
Timeframe: Phase I at 1 month
Intervention Appropriateness
Timeframe: Phase I at 3 months
Intervention Appropriateness
Timeframe: Phase II at 3 months
Intervention Appropriateness
Timeframe: Phase II at 6 months
Intervention Treatment Receipt
Timeframe: Phase I at 1 month
Intervention Treatment Receipt
Timeframe: Phase I at 3 months
Intervention Treatment Receipt
Timeframe: Phase II at 3 months
Intervention Treatment Receipt
Timeframe: Phase II at 6 months