An Assessment of Patient Preference for the Amara View Full Face Mask Compared to the ResMed AirFit F40 -a Benchmark Protocol
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 35
- 试验地点
- 2
- 主要终点
- Patient Preference
研究概览
简要总结
This randomized crossover, benchmark clinical trial aims to compare the Philips Amara View and ResMed AirFit F40 minimal contact full face masks on patient preference of mask attributes and usage parameters. At the first study visit participants will be fitted with either the Amara View or the AirFit F40. The order in which participants will use the masks will be randomized. After the fitting and completion of informed consent, eligibility, and baseline questionnaires, participants will take home the first mask and use it with their prescribed PAP device for 15-days. After the first 15-day time period participants will return for their second visit. At this visit participants will return the first mask to the study team and complete a survey on the mask attributes. They will then be fitted with the second study mask and will be given the mask to take home and use with their prescribed PAP device for 15-days. At the end of the second 15-day trial period, participants will return for the third study visit. At this visit they will return the second mask and complete a mask attributes survey on the second mask.
详细描述
Participants will be recruited via a sleep clinic contracted to recruit participants within the United States. Study staff will be responsible for assessment of inclusion and exclusion criteria. Scheduling will be conducted by the site. Participants who are willing to enroll will be scheduled for an in-person visit to provide informed consent and complete study procedures. During the baseline visit, review the Informed Consent Form (ICF) with the participant explaining and answering any questions the participant may have about the study. If the participant is willing to take part in the study, the ICF will be signed and dated by the participant and the site study representative obtaining consent. Those who provide consent will then complete the Demographics Questionnaire, Baseline Mask Survey, and Eligibility Questionnaire to confirm entry criteria. Participants will be asked to bring their prescribed mask and PAP device to Visit 1.At the initial visit, participants will undergo a fitting of the mask they are randomized to start the study with; either the Amara View or the AirFit F40 mask. Participants will be fit with mask sizes recommended by the clinician. The clinician will use the provided sizing gauges for the Amara View and AirFit F40 masks respectively. Once a mask size is selected for the first study mask, the participant will undergo short trials using his or her own PAP machine at therapeutic pressure, and an assessment of mask fit will be performed. If the participant's PAP device is not available, they will be fitted with the mask and will undergo short trials using a PAP device provided by the site. Participants may be fitted with up to three mask sizes for the mask. A Mask Fitting Survey will be used to capture the participant's prescribed pressure, mask (cushion/frame) sizes and fitting observations for the first study mask.
After the mask fitting, participants will be given the first study mask to take home. They will be encouraged to use the mask for the full 15-days of the first trial period. After the first 15-day trial period with the first study mask, participants will return to the site for their second study visit. Participants will be instructed to bring their PAP device and the first study mask to the visit. Participants will complete a mask attributes survey on the first study mask and then they will be fitted with the second study mask. Fitting procedures will follow the same procedure as described above in the baseline visit. After the mask fitting, participants will be given the second study mask to take home. They will be encouraged to use the mask for the full 15 days of the second trial period. After the second 15-day trial period with the second study mask, participants will return to the site for the third and final study visit. During this visit, participants will complete a mask-attributes survey on the second study mask and return all study product.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- None
盲法说明
N/A - No masking will be performed.
入排标准
- 年龄范围
- 21 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Aged 21-85 years (inclusive)
- •Weight >66 pounds/30 kg
- •Established on PAP for ≥90 days at the time of consent
- •Currently prescribed and using fixed pressure, Auto CPAP, or Bi-Level therapy on a regular basis (average PAP usage of ≥4 hours/night, ≥ 4 days per week for ≥3 months)
- •Currently using a Full-Face mask
- •Able to read, write, speak and understand English
- •Willing and able to provide informed consent
- •Willing and able to follow instructions and complete all activities required by the study
- •Able to remove a sleep apnea mask without assistance
排除标准
- •Currently using a Philips Respironics Amara View FFM or ResMed AirFit F40 FFM
- •Allergy to silicone
- •Allergy to latex
- •Unique facial features (i.e., deformities of the face and/or head, piercings, etc.) that could interfere with the therapeutic use of this type of mask
- •Employee or living with a family member who works for Philips or any company that designs, sells, or manufactures sleep-related products.
- •Prescribed oxygen at night or continuously
- •Recent eye surgery or dry eyes
- •Hiatal hernia
- •Excessive reflux
- •Impaired cough reflux
- •Impaired cardiac sphincter function
- •Using prescription drugs that induce vomiting
- •Currently participating in another interventional research study or planned participation in another interventional clinical research study during the trial period
- •Prescribed an ASV (adaptive servo-ventilation) device
- •Prescribed mechanical ventilation
- •Pre-existing conditions such as bullous lung disease, pathologically low blood pressure, bypassed upper airway, pneumothorax, pneumocephalus, cerebral spinal fluid (CSF) leaks, or cribriform plate abnormalities
- •Any unstable medical condition (e.g., uncontrolled cardiac, lung, or neurological disease) or limitation that would affect the participant's ability to complete trial activities
- •Experiencing any acute illness (e.g., acute sinusitis, ear or eye infections, upper respiratory infections, pharyngitis, bronchitis, pleurisy, pneumonia, or facial dermatitis) that would impact their ability to use the mask and/or PAP therapy during the trial
- •Surgical procedures involving the head, neck, face (eyes, ears, nose), or lungs in the previous 90 days or taking place any time during the trial period
- •Advised by a health care provider to avoid magnets
- •Patient or patient's household member, caregiver or bed partner in close vicinity currently using medical implants or medical devices that would be affected by magnets, including but not limited to:
- •Pacemakers
- •Implantable cardioverter defibrillators (ICD)
- •Neurostimulators
- •Magnetic metallic implants/electrodes/valves placed in upper limbs, torso, or higher (i.e., neck and head)
- •Cerebral spinal fluid (CSF) shunts (e.g., ventriculo peritoneal (VP) shunt)
- •Aneurysm clips
- •Embolic coils
- •Intracranial aneurysm intravascular flow disruption devices
- •Metallic cranial plates, screws, burr hole covers, and bone substitute devices
- •Metallic splinters in the eye
- •Ocular implants (e.g., glaucoma implants, retinal implants)
- •Certain contact lenses with metal
- •Implants to restore hearing or balance that have an implanted magnet (such as cochlear implants, implanted bone conduction hearing devices, and auditory brainstem implants)
- •Magnetic denture attachments
- •Metallic gastrointestinal clips
- •Metallic stents (e.g., aneurysm, coronary, tracheobronchial, biliary)
- •Implantable ports and pumps (e.g., insulin/infusion pumps)
- •Hypoglossal nerve stimulators
- •Devices labeled as MR (Magnetic Resonance) unsafe
- •Magnetic metallic implants not labeled for MR or not evaluated for safety in a magnetic field
- •PAP device is unknown, or they are using a recalled device that has not yet been remediated. Recalled devices include:
- •DreamStation CPAP, Auto CPAP, or BiPAP
- •DreamStation BiPAP, autoSV (ASV)
- •DreamStation ST, AVAPS (Also known as DreamStation BiPAP AVAPS or DreamStation BiPAP S/T)
- •DreamStation Go CPAP, APAP or Auto CPAP
- •Dorma 400 or 500 CPAP or Auto CPAP
- •System One ASV4
- •System One (Q-Series) 50 series CPAP, Auto CPAP, or BiPAP
- •System One (Q-Series) 60 series CPAP, Auto CPAP, or BiPAP
- 另有 2 项未显示
结局指标
主要结局
Patient Preference
时间窗: Up to 35 days
Percentage of patients who prefer the Amara View compared to the AirFit F40 for the following: seal, comfort, stability, noise level, headgear, mask cushion ease of use, less disruptive air venting, and overall preference.
Difference in Net Promotor Score
时间窗: Up to 35 days
Difference in the Net Promotor Score between the Amara View and AirFit F40. The Net Promotor score is based on a 0 to 10 scaled question "Would you recommend this (Amara View FFM or AirFit F40) mask to others?" where 0 indicates "unlikely to recommend" and 10 indicates "likely to recommend". The 0 to 10 scale is grouped into three categories: promoters (ratings 9-10), detractors (ratings 0-6), and neutral (7-8). Net Promoter Scores (NPS) were calculated by subtracting the percentage of detractors from the percentage of promoters: \[% Promoters\] - \[% Detractors\]. Ratings of 7-8 were considered neutral. The NPS scale ranges from -100 to 100. Scores less than 100 indicate that the percentage of detractors exceeds the percentage of promoters. Scores greater than 100 indicate the percentage of promoters exceeds the percentage of detractors. A NPS score of 0 indicates the percentages of promoters and detractors are equal.
Patient Preference on Mask Attributes
时间窗: up to 35 days
Comparison in satisfaction ratings between the Amara View and the AirFit F40 on mask attributes including: bed partner satisfaction, fit, comfort, ability to maintain a seal during use, stability of the mask, noise level, air venting, comfort of breathing, sleep quality, visual appeal, and overall satisfaction. The scale for each mask attribute ranges from 0 to 10, where 0 indicates the lowest satisfaction and 10 indicates highest satisfaction. Each mask attribute was rated and analyzed individually; the scores from the separate mask attributes were not totaled.
Ease of Use
时间窗: up to 35 days
Ease of use and satisfaction ratings between the Amara View and the AirFit F40 on the following parameters: mask clips, mask overall, assembly, disassembly. The scale for each ease-of-use attribute ranges from 0 to 10, where 0 indicates the most difficult and 10 indicates the easiest. Each ease-of-use attribute was rated and analyzed individually; the scores from the separate attributes were not totaled.
Difference in Net Promotor Score
时间窗: Up to 35 days
Difference in the Net Promotor Score between the Amara View and AirFit F40. The Net Promotor score is based on a 0 to 10 scaled question "Would you recommend this (Amara View FFM or AirFit F40) mask to others?" where 0 indicates "unlikely to recommend" and 10 indicates "likely to recommend". The 0 to 10 scale is grouped into three categories: promoters (ratings 9-10), detractors (ratings 0-6), and neutral (7-8). Net Promoter Scores (NPS) were calculated by subtracting the percentage of detractors from the percentage of promoters: \[% Promoters\] - \[% Detractors\]. Ratings of 7-8 were considered neutral. The NPS scale ranges from -100 to 100. Scores less than 100 indicate that the percentage of detractors exceeds the percentage of promoters. Scores greater than 100 indicate the percentage of promoters exceeds the percentage of detractors. A NPS score of 0 indicates the percentages of promoters and detractors are equal.
Patient Preference
时间窗: Up to 35 days
Percentage of patients who prefer the Amara View compared to the AirFit F40 for the following: seal, comfort, stability, noise level, headgear, mask cushion ease of use, less disruptive air venting, and overall preference.
次要结局
- Leak(up to 35 days)
- Adherence to PAP Therapy(up to 35 days)
- Leak(up to 35 days)
- Number of Sleep Apnea Events Per Hour Measured by the Residual Apnea Hypopnea Index (AHI)(up to 35 days)
- Air Pressure(30 days)
- Adherence to PAP Therapy(up to 35 days)