- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07765381
A Clinical Trial to Evaluate the Effects of a Supplement on Symptoms Associated With Hormone Imbalance
This study evaluates the effects of the Love Wellness Hello Burn, Balance supplement on symptoms associated with hormone imbalance, as measured by energy levels and healthy eating choices and habits. The trial is a single-arm, open-label, virtual study conducted over 4 weeks, in which all 40 enrolled participants will take the test product daily.
Participants will complete self-reported questionnaires at Baseline, after First Use (within 1-3 hours of use), and at Weeks 1, 2, 3, and 4 to assess changes in symptoms associated with hormonal imbalance, energy levels, healthy eating choices and habits, metabolism, and overall product efficacy.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Nevada
-
Las Vegas, Nevada, Estados Unidos, 89101
- Citruslabs
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Be female
- Be aged 25 or over
- Has in the past 4 weeks experienced issues regarding all of the following: difficulty making healthy eating choices and habits, hormonal-driven challenges with healthy eating choices and habits, self-perceived slow metabolism, and low energy
- Generally healthy - does not live with any uncontrolled chronic disease
- If taking oral over-the-counter supplements or herbal remedies targeted at hormone balance or energy, has been consistently taking these for at least 3 months prior to starting the study and is willing to maintain this routine for the study duration
- Willing to refrain from introducing any products or any new forms of prescription medication or supplements that target hormone balance or energy for the study duration
- Willing to maintain their diet, sleep schedule, and activity level for the duration of the study
- Not currently partaking in another research study and will not be partaking in any other research study for the next 4 weeks and at any point during this study's duration
- Resides in the United States
Exclusion Criteria:
- Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
- Anyone currently taking a prescription thyroid treatment (like levothyroxine)
- Anyone with known severe allergic reactions
- Anyone with any allergies or sensitivities to any of the study product ingredients
- Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
- Anyone diagnosed with diabetes (type I or type II)
- Anyone unwilling to follow the study protocol
- Has changed birth control in the past 3 months
- Anyone planning to undergo any surgeries or invasive treatments during the study duration
- Anyone who has had any major illness in the last 3 months
- Anyone with a history of substance abuse
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Hello Burn, Balance Supplement
|
All participants take 2 capsules of the Love Wellness Hello Burn, Balance supplement once daily in the morning with a glass of water during the first meal of the day for 4 weeks.
The supplement contains selenium (as L-selenomethionine) 55 mcg, chromium (as chromium polynicotinate) 35 mcg, Hello Burn Blend (L-carnitine tartrate, organic green tea leaf powder) 1250 mcg, hypromellose capsule, microcrystalline cellulose, and magnesium stearate.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in Symptoms Associated with Hormone Imbalance
Periodo de tiempo: Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Assessed via self-reported questionnaire measuring participant-perceived symptoms associated with hormonal imbalance
|
Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in Energy Levels
Periodo de tiempo: Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Assessed via self-reported questionnaire measuring participant-perceived energy levels
|
Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
|
Change in Healthy Eating Choices
Periodo de tiempo: Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Assessed via self-reported questionnaire measuring participant-perceived healthy eating choices and including stress eating
|
Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
|
Change in Perception of Metabolism
Periodo de tiempo: Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Assessed via self-reported questionnaire measuring participant-perceived metabolic rate
|
Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
|
Product Efficacy Perception
Periodo de tiempo: Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Assessed via self-reported questionnaire measuring participant perception of the test product's overall efficacy
|
Baseline, First Use (within 1-3 hours of use), Week 1, Week 2, Week 3, and Week 4
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- 20688
- legacy-20688
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .