Satisfaction
Conditions
Brief summary
This study assesses to determine the most effective type of device on the degree of satisfaction of patients with amyotrophic lateral sclerosis for managing oral self-biting injuries. Thirty-one patients with amyotrophic lateral sclerosis will wear two devices, a hard occlusal splint (HOS) and a flexible customized mouthguard (FCM), for two weeks each one. The sequence will be randomized to obtain one-half of the participants starting the first week wearing the HOS, and the other half wearing the FCM. The participants will rate the degree of satisfaction with the device and the degree of improvement or worsening of oral self-biting injuries in a 10-point scale. They will also rate the degree of change in their quality of life because of changes in their oral self-biting injuries. Finally they will rate the compliance and report the adverse effects.
Detailed description
This crossover intervention study aims to assess the most effective type of device on the degree of satisfaction of patients with amyotrophic lateral sclerosis for managing oral self-biting injuries. Thirty-one patients with amyotrophic lateral sclerosis diagnosed in the ALS Functional Unit at Bellvitge University Hospital will participate in this randomized crossover trial. Two devices will be prepared for each patient, a hard occlusal splint (HOS) and a flexible customized mouthguard (FCM). They will wear one type of device for the first two weeks, followed by a week off, and the other type of device for the fourth and fifth week. The sequence will be randomized to obtain one-half of the participants starting the first week wearing the HOS, and the other half wearing the FCM. The participants will rate the degree of satisfaction with the device in a 10-point scale, considering 0 extremely dissatisfied and 10 completely satisfied, and the degree of improvement or worsening of oral self-biting injuries, considering 0 an extreme worsening and 10 completely improved. They will also rate the degree of change in their quality of life (nothing, a bit, quite, a lot) because of changes in their oral self-biting injuries. Finally they will rate the compliance as the percentage of time the device was used with respect to the recommended time and report the adverse effects (excessive salivation, dry mouth, tooth pain, mucosal irritation, temporomandibular joint (TMJ) pain, TMJ sounds, bite change, other).
Interventions
DEVICEHard occlusal splint
Use of a hard occlusal splint at times they considered helpful.
DEVICEFlexible customized mouthguard
Use of a flexible customized mouthguard at times they considered helpful.
Sponsors
University of Barcelona
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients with amyotrophic lateral sclerosis diagnosed in the ALS Functional Unit at Bellvitge University Hospital.
Exclusion criteria
* Patients who cannot be treated due to the advanced evolution of their disease.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Degree of satisfaction using a questionnarie | 1-2 weeks | Participant satisfaction will be assessed by asking the question How satisfied are you with the device? using a 0-10 point scale (considering 0= extremely dissatisfied and 10 = completely satisfied) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Degree of improvement or worsening of oral self-biting injuries using a questionnarie | 1-2 weeks | The degree of improvement or worsening of oral self-biting injuries while using the device will be assessed by asking the question How much do you think wearing the device improves the oral self-biting injuries? using a 0-10 point scale (considering 0= extreme worsening to 10= completely improved). |
| Degree of change in their quality of life using a questionnaire | 1-2 weeks | The degree of change in their quality of life while using the device because of changes in their oral self-biting injuries will be assessed by asking the question How much do you think wearing the device improves your quality of life? using a 4-point scale (considering 0 = nothing, 1 = a bit, 2 = quite, 4 = a lot). |
| Compliance | 1-2 weeks | Participants compliance using the device will be assessed as the percentage of time the device was used with respect to the recommended time. |
| Adverse effects | 1-2 weeks | The adverse effects related to use of the device will be recorded (excessive salivation, dry mouth, tooth pain, mucosal irritation, temporomandibular joint (TMJ) pain, TMJ sounds, bite change, other). |
| Willingness to pay | 1-2 weeks | Participants willingness to pay will be assessed by asking the question What is the maximum you would pay for the device? |
Countries
Spain
Contacts
Primary ContactNina Riera-Punet, DDS PhD
Outcome results
None listed