Multidimensional Sleep Health Intervention for Couples
The goal of this pilot dyadic study is to adapt a multidimensional sleep health (MDSH) intervention, previously disseminated at the individual level, for relationship partners, determine whether it improves sleep health and aspects of cardiometabolic health, and understand the role of dyadic dynamics in intervention ef
| Condition(s) | Blood Pressure, Sleep, Cardiovascular Health |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The goal of this pilot dyadic study is to adapt a multidimensional sleep health (MDSH) intervention, previously disseminated at the individual level, for relationship partners, determine whether it improves sleep health and aspects of cardiometabolic health, and understand the role of dyadic dynamics in intervention effects. Can a dyadic MDSH intervention improve sleep health and blood pressure (primary outcomes) in relationship partners? Can a dyadic MDSH intervention improve anthropometric markers of adiposity, psychosocial indicators, stress, dyadic adjustment and coping, self-rated health (secondary outcomes) in relationship partners? As this is a single-arm study, there is no control group. All relationship partners will complete a three-tier screening process, attend two in-person vi |
| Who can participate | Inclusion Criteria: * Adults aged 30-65 years * English-speaking * Systolic blood pressure greater than or equal to 120 mmHg (at minimum one individual in dyad) * Sub-optimal sleep health (at minimum short/long sleep duration and/or irregular sleep patterns) Exclusion Criteria: * Optimal sleep health * History of cardiovascular disease or cancer * Not cognitively able to complete study requirements * Known medical conditions that would prevent them from safely participating in the study (severe psychiatric disorders, neurological degenerative disease, substance abuse/dependence) * History of severe depression or high risk of sleep apnea/use of a Continuous Positive Airway Pressure (CPAP) device * Inability to provide informed consent |
| Ages | 30 Years to 65 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Columbia University |
| Locations | New York, New York, United States |
| Start date | 2026-06-08 |
| NCT ID | NCT07603245 |
| Official listing | https://clinicaltrials.gov/study/NCT07603245 |