Community Intervention to Improve Depressive Symptoms Among Older Adults (VIDACTIVA)

NCT ID: NCT06065020

Last Updated: 2025-02-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 64 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-10-23
• Study Completion Date: 2025-02-03

Brief Summary

The goal of this pilot trial is to test how feasible is to conduct a large clinical trial that evaluate both implementation and effectiveness outcomes of a community-based interventions for older adults with depression in low-resource urban settings from Lima, Peru.

The main questions:

Is the way we are planning the study, including those who are taking part and what they will do, good for a large study?

Is the interventional package we are developing good the way it is, and can it be done the way we planned it?

Detailed Description

Participants who join will be split into two groups: one group will get the interventional program, and the other group will get standard care. In the interventional group, community health workers will meet with participants eight times to do activities and talk about how they feel. The standard group will have two visits where they will learn things about mental health.

The results of the study will help the researchers understand whether they can test the program in larger study. Additionally, see whether those participants in the interventional group feel better than those who are in the standard group.

Sample size: This is a pilot trial. No sample size calculations are needed because the objective is NOT to evaluate the effect of the intervention, but rather the feasibility of conducting a large-scale clinical trial. It is expected to enroll 64 participants (32 control group vs 32 intervention group). This number is based on previous formative study and training of community health workers.

Researchers will collect basic information to assess feasibility for a larger trial, including:

• Number of potential participants screened per month;
• Number of participants enroled per month;
• Average time from enrolment to randomisation.
• Average time to reach enrolment goal
• Proportion of eligible participants who enrol
• Proportion of people who maintain the study in both groups.
• Reasons for abandoning the study.
• Visit durations

Conditions

Depression, Anxiety

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Intervention group

VIDACTIVA program

Group Type: EXPERIMENTAL

VIDACTIVA sessions

Intervention Type: BEHAVIORAL

Community health workers (CHWs) will delivered VIDACTIVA intervention that consists in 8 home-sessions, one hour duration, within a period of 14 weeks + 2 follow-up calls (monthly). In total, a period of 22 weeks.

The multicomponent intervention consist in the following:

Problem-Solving Exercises: These are basic structured exercises aimed at training older individuals in problem-solving. This activity is centered around the older adult, meaning the older adults guides this activity, and the CHWs is a facilitator.

Physical Activation: This component involves planning and "scheduling" enjoyable activities (physical or social) that the older adult chooses based on their preferences and capabilities.

Education on Depressive Symptoms (psychoeducation)

Control group

Standard Care

Group Type: ACTIVE_COMPARATOR

Standard Care

Intervention Type: BEHAVIORAL

Study fieldworkers will provide 2 educational sessions (45-60 min) about mental health at old age and participant will be guided to mental health community services (primary care centers). One session after the enrolment (week 1) and one at the 14th week.

Interventions

VIDACTIVA sessions

Community health workers (CHWs) will delivered VIDACTIVA intervention that consists in 8 home-sessions, one hour duration, within a period of 14 weeks + 2 follow-up calls (monthly). In total, a period of 22 weeks.

The multicomponent intervention consist in the following:

Problem-Solving Exercises: These are basic structured exercises aimed at training older individuals in problem-solving. This activity is centered around the older adult, meaning the older adults guides this activity, and the CHWs is a facilitator.

Physical Activation: This component involves planning and "scheduling" enjoyable activities (physical or social) that the older adult chooses based on their preferences and capabilities.

Education on Depressive Symptoms (psychoeducation)

Intervention Type: BEHAVIORAL

Standard Care

Study fieldworkers will provide 2 educational sessions (45-60 min) about mental health at old age and participant will be guided to mental health community services (primary care centers). One session after the enrolment (week 1) and one at the 14th week.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Having depressive symptoms (score equal to or greater than 6 on the Patient Health Questionnaire - PHQ 9).
• Capacity to give consent.
• Current residence in Villa El Salvador, Lima, Peru.

Exclusion Criteria

• Previous diagnosis of bipolar disorder
• History of substance abuse
• History of dissociative disorder, psychosis or dementia, or moderate memory and/or cognition problems.

• Minimum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Asociacion Benefica Prisma

OTHER

Sponsor Role: collaborator

Johns Hopkins University

OTHER

Sponsor Role: collaborator

University of Washington

OTHER

Sponsor Role: collaborator

Universidad de San Martín de Porres

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Oscar Flores-Flores, MD, MSc

Role: PRINCIPAL_INVESTIGATOR

Universidad de San Martin de Porres

Locations

Universidad de San Martin de Porres

Lima, Lima Province, Peru

Countries

Peru

References

Cruz-Riquelme T, Zevallos-Morales A, Carrion I, Otero-Oyague D, Patino V, Lastra D, Valle R, Parodi JF, Pollard SL, Steinman L, Gallo JJ, Flores-Flores O. Pilot trial protocol: community intervention to improve depressive symptoms among Peruvian older adults. Pilot Feasibility Stud. 2024 Aug 22;10(1):112. doi: 10.1186/s40814-024-01540-1.

Reference Type: DERIVED

PMID: 39175082 (View on PubMed)

Other Identifiers

E10012021018

Identifier Type: -

Identifier Source: org_study_id