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Behavioral Activation, Nutrition, and Activity Intervention

Multi-Component Behavioral Activation, Nutrition, and Activity Intervention for Persons Aging With HIV

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06239961
Enrollment
7
Registered
2024-02-02
Start date
2024-09-23
Completion date
2025-06-19
Last updated
2025-07-04

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

Conditions

HIV

Keywords

Aging, HIV, Social engagement, Nutrition, Physical activity

Brief summary

This study will explore if a behavioral intervention program to assist people aged 50 and older with HIV is practical. The program includes a coach who talks with participants, encouraging them to be more active, reduce loneliness, and eat healthier.

Detailed description

This study aims to see if a 12-week program called Behavioral Activation (BA) can help people aged 50 and above with HIV by reducing loneliness and boosting social engagement. The program includes physical activity and nutrition guidance and is led by remote coaches. Investigators will recruit participants from the University of Maryland THRIVE program and other HIV centers in Baltimore. Investigators will test the program with 10 people aged 50 and above with HIV to see if it works. If it proves to be helpful and accepted, investigators might move on to a larger study to evaluate it more thoroughly.

Interventions

BEHAVIORALSocial Connection

6 weekly Behavioral Activation Intervention calls with a 1 hour duration for each call.

4 weekly nutritional coaching calls with a Registered Dietician with a 1 hour duration for each call.

4 weekly physical activity coaching sessions with a 1 hour duration for each call.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
University of Maryland, Baltimore
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

The Brief Behavioral Activation (BA) Coaching will involve having lay coaches work with participants remotely (i.e., by phone or videoconference) to identify and schedule values-based, rewarding social engagement and activities and to use strategies to reduce and problem-solve barriers to social connectedness. Participants first review their daily activity patterns, and then chose activity goals, worked on specific implementation plans, and reviewed their successes and areas for improvement. The behavioral activation coach program will be modified to address the needs of people aging with HIV (PAWH) by working with those in the community to tailor the content and mode of delivery. There will be additional modules on physical activity and nutrition.

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. 50 years of age or older 2. HIV positive diagnosis 3. Montreal Cognitive Assessment score \> 13 4. Report minimal level of loneliness, isolation, and/or depression (PHQ9 \> 5) 5. Able to consent 6. Ability to read or speak English 7. Attend the UM THRIVE Center or another HIV center in Baltimore

Exclusion criteria

1\) No severe cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
DepressionBaseline and Week 16Participants will complete the Patient Health Questionnaire - 9 (PHQ-9) at baseline and at the Week 16 follow up visit. The nine items of the PHQ-9 are based directly on the nine diagnostic criteria for major depressive disorder in the DSM-IV. Where total scores of 5 to 9 = mild, 10 to 14 = moderate, 15 to 19 = moderately severe, and 20 = severe depression.
LonelinessBaseline and Week 16Participants will complete the University of California, Los Angeles (UCLA) Loneliness Questionnaire (Version 3) at baseline and at the Week 16 follow up visit. This is a 20-item scale designed to measure one's subjective feelings of loneliness. Participants rate each item on a scale where 1 = Never, 2 = rarely, 3 = sometimes and 4 = Often. Total scores of 20 - 40 are considered low to moderate, 40 - 60 are considered moderate to high, and score above 60 are considered high in terms of loneliness.
Social IsolationBaseline and Week 16Participants will complete the Patient-Reported Outcomes Measurement Information System (PROMIS) Social Isolation Scale at Baseline and at the Week 16 follow up visit, to measure social isolation. Total scores of 0.5 - 1.0 SD (standard deviation) worse than the mean = mild symptoms/impairment, scores of 1.0 - 2.0 SD worse than the mean = moderate symptoms/impairment, and scores 2.0 SD or more worse than the mean = severe symptoms/impairment.
Physical Activity (actigraphy) stepsBaseline and Week 16Participants will be given a wearable sensor device to track movements. Physical activity will be assessed using number of daily steps walked measured by the wearable sensor.
Physical Activity (actigraphy) sedentary timeBaseline and Week 16Participants will be given a wearable sensor device to track movements. Physical inactivity will be assessed using minutes of sedentary time measured by a wearable sensor.
Total Sleep Time (TST) with ActigraphyBaseline and Week 16TST will be measured by a wearable sensor, from baseline to the final week of the intervention.
Sleep Efficiency (SE) with ActigraphyBaseline and Week 16SE will be measured by a wearable sensor, from baseline to the final week of the intervention.
Sleep Onset Latency (SOL) with ActigraphyBaseline and Week 16SOL will be measured by a wearable sensor, from baseline to the final week of the intervention.
Nutritional IntakeBaselineParticipants will complete the 18-item Mini Nutritional Assessment (MNA®) at the baseline visit. The MNA® is a screening tool to help identify elderly persons who are malnourished or at risk of malnutrition. A score of 12 or greater indicates the person is well nourished and needs no further intervention. A score of 8-11 indicates the person is at risk of malnutrition. A score of 7 or less indicates the person is malnourished.

Secondary

MeasureTime frameDescription
EducationBaselineSelf reported completed level of schooling or degree obtained.
CD4 countBaselineA lab measurement of immune function in patients living with HIV.
HIV viral loadBaselineViral load is a marker of response to antiretroviral therapy (ART).
Bone Mineral Density (BMD)BaselineBMD is expressed by the mass of calcium hydroxyapatite present in a given area or volume of bone in a unit of mass/area (g/cm2) or mass/volume (g/cm3), respectively. -2.5 and below = Osteoporosis -1.1 to -2.5 = Osteopenia.
Smoking StatusBaselineParticipants self reported smoking usage.
Blood pressureBaselineMeasurement of the force of blood against the arterial walls, to evaluate the impact of interventions on cardiovascular health.
Generalized Anxiety Disorder 7Baseline and Week 16Participants will complete the Generalized Anxiety Disorder scale-7 (GAD-7) at the baseline and week 16 follow up visit. It is a seven-item diagnostic tool, based on the Diagnostic and Statistical Manual of Mental Disorders-IV (DSM-IV) criteria, for identifying likely cases of GAD. Where a score of 0 - 4 = minimal anxiety, 5 - 9 = mild anxiety, 10 - 14 = moderate anxiety, and a score greater than 15 = severe anxiety.
Diabetes statusBaselineAssessing participants for the presence or absence of diabetes.
Aspirin usageBaselineAssessing whether participants are using aspirin.
Statin usageBaselineAssessing whether participants are using statin medications.
ASCVD Risk ScoreBaseline10-year risk calculated using the cardiovascular disease risk measures listed to help decide Statin or Aspirin prescription.
Urine AlbuminBaselineUrine analysis detects protein and blood in urine, supposed to be filtered by kidney, where Abnormal = Risk for renal disease; \>30 = Kidney disease.
Glomerular Filtration RateBaselineMeasures kidney performance based on the amount of blood filtered per minute. Abnormal = Risk for renal disease; \<60 = Kidney disease; \<=15 = Kidney failure.
Lipids (Total cholesterol, Low-density lipoprotein (LDL), High-density lipoprotein (HDL), Triglycerides (TG))BaselineLipid panel measures all three cholesterol and triglyceride/fat in the blood to assess for CVD risk. \>240 mg/dl = High total cholesterol; 130 - 159 md/dl = High LDL; \<40 mg/dl = Low HDL; \>150 mg/dl = High TG.
Late Life Function and Disability InstrumentBaseline and Week 16Participants will complete the Late-Life Function & Disability Instrument (Late-Life FDI). It is designed to assess and be responsive to meaningful change in two distinct outcomes: function and disability. Scores approaching 100 signify high levels in ability to perform discrete actions and activities (without assistance), scores approaching 0 signify low levels in ability to perform discrete actions and activities (without assistance).
Engagement in activitiesBaseline and Week 16Participants will complete the Yale Physical Activity Survey. This survey was developed to determine the type, amount and patterning of physical activity/exercise in older adults. The tool is composed of two sections - (1) amount of physical activity/exercise performed during a typical week in the past month and (2) activities performed in the past month. In section one, participants are handed a checklist of activity categories (work, exercise, and recreational activities) and are asked how often during the past week they performed a particular activity from each category. Higher scores indicate high levels of physical activity, while lower score indicate lower activity levels or more sedentary lifestyle.
Reece 9-item HIV-related Stigma ScaleBaseline and Week 16A 9-item instrument with possible scores ranging from 0 (no perceived stigma) to 45 (high perceived stigma). The HIV Stigma Scale was designed to measure the perception of stigma by those who are HIV infected.
AgeBaselineSelf reported chronological date of birth.
RaceBaselineSelf reported racial or ethnic background.
Gender at birthBaselineCharacterization of male or female based on their biological characteristics when they were born.
Gender identity nowBaselineCharacterization of male or female based on their self-identified gender.
Sexual preferenceBaselineParticipants self reported sexual orientation.

Countries

United States

Outcome results

None listed

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