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Phase 4 of Designed With You

Building Active Living and Addressing Needs for Caregiver Empowerment (BALANCE) Study - Phase 4 of Designed With You

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07157995
Acronym
BALANCE
Enrollment
20
Registered
2025-09-05
Start date
2026-01-01
Completion date
2026-10-30
Last updated
2026-07-02

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

Conditions

Disability Physical

Keywords

Caregivers, Disability, Sensory Disability, Mobility Disability

Brief summary

The purpose of this study is to provide evaluate the feasibility of a structured 8-10-week, multi-component intervention that integrates individualized resource navigation, personalized self-care planning, emergency and end of life (EOL) preparedness, and peer support to improve the well-being, resource access and social connectedness of caregivers with disabilities. For this study we are interested in caregivers over the age of 18 who have some form (e.g. mobility or sensory) disability and are caring for a person with a disability and/or a chronic illness.

Detailed description

The BALANCE is a feasibility study of the BALANCE intervention and will be delivered over 8-10 weeks. The proposed study is a Phase 1 feasibility trial designed to assess the feasibility and acceptability of a novel intervention aimed at \[briefly describe intervention\]. The primary objectives are to evaluate the practicality of implementing the intervention, participant engagement, and the appropriateness of study procedures. Given the early-stage nature of this research, a control group is not required. Phase 1 feasibility studies are not intended to assess efficacy or comparative outcomes, but rather to refine the intervention and study logistics. According to guidance from the Office of Research Integrity (ORI), "Phase I trials are feasibility trials focused on developing and pretesting the acceptability, feasibility, and safety of the intervention components of Balance. "No control condition is needed."14 This approach aligns with best practices in early intervention development and allows for iterative refinement before proceeding to more rigorous testing in later phases (e.g., randomized controlled trials).

Interventions

BEHAVIORALBALANCE Building Active LIving and Addressing Needs for Caregiver Empowerment

The Balance intervention will include individual visits by a Caregiver Navigator and group sessions with other participants, led by the caregiver navigator. The focus will be on future planning, resources for unmet needs and support and socialization.

Sponsors

Johns Hopkins University
Lead SponsorOTHER
National Institute on Disability, Independent Living, and Rehabilitation Research
CollaboratorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

feasibility study of the BALANCE intervention

Eligibility

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

Inclusion criteria

* 18 years of age and older, * Community dwelling in the state of Maryland, * Self report of physical or sensory disability and * self-report of serving as a family caregiver for a person for at least 10 hours/week.

Exclusion criteria

* have a terminal diagnosis (\<1 year expected survival), and * \> severe cognitive impairment (5-7 errors) based on the Short Portable Mental Status Questionnaire (SPMQ)

Design outcomes

Primary

MeasureTime frameDescription
Perceived Stress ScaleBaseline and post intervention at approximately 10 weeksMeasurement of perceived stress. Scores can range from 0 to 40, with higher scores indicating worse levels of perceived stress.
Caregiver Burden Short FormBaseline and post intervention at approximately 10 weeksMeasure to address burdensome activities related to care giving experiences. Total score ranges from 0-48 wit higher scores indicating greater caregiver burden.
Depressive Symptoms (PHQ-9)Baseline and post intervention at approximately 10 weeksMeasure of depressive symptoms. Score range 0-27, higher values represent more depression symptoms

Countries

United States

Contacts

CONTACTJaniece Taylor, PhD, RN
jwalke90@jhu.edu443-287-4503
CONTACTAlicia Cooke
acooke8@jhu.edu4109559954
PRINCIPAL_INVESTIGATORJaniece Taylor, PhD, RN

Johns Hopkins University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 3, 2026