Anxiety State, Depressive Symptoms, Mild Cognitive Impairment
Conditions
Keywords
Homebound Older Adults, Mild Cognitive Impairment, Depressive and Anxious Symptomatology, Cognitive-Emotional Intervention, Randomized Controlled Trial
Brief summary
The main goal of this research is to assess the efficacy of a 10-week home-delivered cognitive-emotional intervention program for homebound older adults presenting Mild Cognitive Impairment (MCI) and depressive and/or anxiety symptoms. The Homebound Elderly People Psychotherapeutic Intervention (HEPPI) combines cognitive training, psychotherapeutic techniques, and compensatory strategy training, and was designed to optimize memory function and to reduce depressive or anxious symptomatology of these older adults. A two-arm randomized controlled trial (RCT) is conducted to investigate the efficacy of the HEPPI among the homebound older population.
Detailed description
The present study aims to assess the efficacy of a cognitive-emotional intervention (the HEPPI program) for homebound older adults with MCI and depressive and/or anxious symptomatology. The research design of the trial followed the methodological recommendations for conducting goropsychoterapy research. Moreover, a pilot RCT was conducted prior to the present RCT, in order to assess the feasibility, acceptability, and preliminary efficacy of the HEPPI. Appropriate adjustments to the HEPPI protocol were carried out considering the results. The present study is a two-arm RCT comparing the intervention condition (HEPPI) to a treatment as usual (TAU) control group. The sample includes community-dwelling older adults who do not leave home more often than once a week. Homebound older adults are recruited from the community through contact with their health care networks. A minimum number of 79 participants per condition will be required (N=158). Accounting for an expected 20% attrition rate, an anticipated sample of 198 participants will be enrolled in the study. Participants who demonstrate interest in the study are informed of the goals and procedures of the research and asked to provide informed consent before eligibility assessment. Eligible participants are randomly assigned to the HEPPI or the TAU group. Homebound older adults are asked to complete baseline, post-intervention, and 3-month follow-up assessments. Assessments include neuropsychological tests to assess cognition function, psychological health, subjective memory complaints, quality of life, functional status, perceived loneliness, and personality. The study procedures take place at the participants' homes.
Interventions
BEHAVIORALHEPPI
Homebound Elderly People Psychotherapeutic Intervention
Sponsors
Foundation for Science and Technology, Portugal
University of Coimbra
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Homebound older adults aged 65 years and older; * MoCA score 1 to 1.5 standard deviation below the mean for age- and education- adjusted norms; * FCSRT total immediate and delayed recall scores ≤ 35 and ≤ 12, respectively; * Presence of subjective memory complaints (SMCS score ≥ 3); * Presence of depressive symptomatology (GDS-30 score ≥ 11); * Presence of anxious symptomatology (GAI score ≥ 8); * No significant impact from cognitive impairment on daily functional capacity; * Residence in mainland Portugal;
Exclusion criteria
* Presence or history of significant neurological conditions; * Presence of severe psychiatric illnesses; * Presence of comorbid medical conditions associated with cognition decline; * Use of psychotropic medication for less than three months; * Presence of alcoholism or toxicomania; * Significant impairment of vision, hearing, communication, or manual dexterity.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Anxious Symptomatology | Baseline, post-intervention, and 3-month follow-up | Measured by Geriatric Anxiety Inventory (GAI) \| Lower scores indicate a better outcome |
| Changes in Episodic Memory | Baseline, post-intervention, and 3-month follow-up | Logical Memory of the Wechsler Memory Scale-III (LM) \| Higher scores indicate a better outcome |
| Changes in Depressive Symptomatology | Baseline, post-intervention, and 3-month follow-up | Measured by Geriatric Depression Scale-30 (GDS-30) \| Lower scores indicate a better outcome |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Subjective Memory Complaints | Baseline, post-intervention, and 3-month follow-up | Measured by Subjective Memory Complaints Scale (SMCS) \| Lower scores indicate a better outcome |
| Changes in Perceived Quality of Life | Baseline, post-intervention, and 3-month follow-up | Measured by European Portuguese World Health Organization Quality of Life-Old Module (WHOQOL-OLD) \| Higher scores indicate a better outcome |
| Changes in Loneliness | Baseline, post-intervention, and 3-month follow-up | Measured by UCLA Loneliness Scale (UCLA) \| Lower scores indicate a better outcome |
| Changes in Functional Status | Baseline, post-intervention, and 3-month follow-up | Measured by Adults and Older Adults Functional Assessment Inventory (IAFAI) \| Lower scores indicate a better outcome |
| Changes in General Cognitive Function | Baseline, post-intervention, and 3-month follow-up | Measured by Addenbrooke's Cognitive Examination-Revised (ACE-R) \| Higher scores indicate a better outcome |
| Changes in Attentional Control | Baseline, post-intervention, and 3-month follow-up | Measured by Digit Symbol-Coding of the Wechsler Adult Intelligence Scale-III (DSC) \| Higher scores indicate a better outcome |
Other
| Measure | Time frame | Description |
|---|---|---|
| Personality Traits | Baseline | Measured by NEO Five-Factor Inventory (NEO-FFI) |
Countries
Portugal
Outcome results
None listed