Johns Hopkins School of Nursing
Baltimore, Maryland, 21205, United States
Location status: Recruiting
NCT Number: NCT07157995
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Baltimore, Maryland, 21205, United States
Location status: Recruiting
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).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: Baseline and post intervention at approximately 10 weeks
Measurement of perceived stress. Scores can range from 0 to 40, with higher scores indicating worse levels of perceived stress.
Time frame: Baseline and post intervention at approximately 10 weeks
Measure to address burdensome activities related to care giving experiences. Total score ranges from 0-48 wit higher scores indicating greater caregiver burden.
Time frame: Baseline and post intervention at approximately 10 weeks
Measure of depressive symptoms. Score range 0-27, higher values represent more depression symptoms
Contact information is provided by the study sponsor or research team.
Alicia Cooke
CONTACT
Janiece Taylor, PhD, RN
CONTACT
Johns Hopkins University
Other
Building Active Living and Addressing Needs for Caregiver Empowerment (BALANCE) Study - Phase 4 of Designed With You
Acronym: BALANCE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07141342
Body Weight, Disability Physical
Pittsburgh, Pennsylvania, United States
View Trial DetailsNCT06326905
Behavior, Behavioral Symptoms
Baltimore, Maryland, United States
View Trial DetailsNCT07603076
Cardiovascular Diseases, Connective Tissue Diseases
Istanbul, Uskudar, Turkey (Türkiye)
View Trial DetailsNCT07671807
Disability Physical
Kaohsiung City, Taiwan
View Trial Details