- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT06234228
Examining Bluetooth Haptic Device Use for Pain and Distress Reduction in Vascular Access Procedures (VA+BHD)
Examining Bluetooth Haptic Device Use for Pain and Distress Reduction in Vascular Access Procedures (VA+BHD)
This pragmatic, randomized study seeks to evaluate the applications of a novel vibrating device for reducing pediatric anxiety and distress during vascular access procedures.
연구 개요
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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California
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Palo Alto, California, 미국, 94304
- Lucile Packard Childrens Hospital Stanford
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Between age 4-99
- Will undergo a vascular access procedure
- English speaking participant and parent or LAR
Exclusion Criteria:
- Legal guardian not present to obtain consent
- Child is unable to self-report pain or anxiety
- Child with a significant neurological condition, or major developmental disability
- Child with active infection of the hand or arm
- Major surgery within the last 48 hours
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 지지 요법
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: BHD synced with mobile game
At the beginning of the vascular access procedure, the BHD will be applied 5 cm above the needle insertion site and maintained in place throughout the procedure. It delivers a constant low-frequency vibration as well as tactile feedback from the game (GF). |
The BHD delivers a constant low-frequency vibration as well as tactile feedback from the game (GF). |
|
다른: BHD only
The participant will wear the BHD 5 cm above the needle insertion site for the duration of the procedure. The BHD will deliver constant low-frequency vibration (CF). |
The BHD will deliver constant low-frequency vibration (CF). |
|
간섭 없음: Standard of Care
The participant will not receive the BHD device. Participant will receive standard of care treatment. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
External observation for pain and anxiety using OBSD-r scale
기간: during vascular access procedure
|
OBSD-r contains 8-item scale assessing participant's affective state; Information Seeking, Crying, Screaming, Restraint, Verbal Resistance, Emotional Support, Verbal Pain and Flail. |
during vascular access procedure
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
modified induction compliance checklist (mICC)
기간: during vascular access procedure
|
The mICC score will be recorded by the trained research observers during the vascular access procedure. Perfect compliance (score of 0) was compared to those that lacked cooperation. mICC will be rated at the time of intervention and only requires one RA. |
during vascular access procedure
|
|
External observation for pain and anxiety using HRAD scale
기간: during vascular access procedure
|
HRAD contains 5-item scale assessing participant's affective state; happy, relaxed, anxious, distressed, with a yes/no answer to cooperation. |
during vascular access procedure
|
|
Faces Pain Scale-Revised for patients aged 4-11
기간: during vascular access procedure
|
Detailed qualitative review of cognitive interview probes with question-by-question analysis of transcribed cognitive interviews to assess for basic comprehension and appropriate use of the FPS-R. This scale is measured from 0-10, where 0 = no pain and 10 = very much pain. |
during vascular access procedure
|
|
Numerical Rating Pain Scale (NRPS) for patients aged 12-17
기간: during vascular access procedure
|
NRPS is a 11-point (0-10) Numeric Rating Pain Scale (NRPS), where 0 = no pain and 10 = worst possible pain. |
during vascular access procedure
|
|
Self formulated procedural satisfaction survey (Healthcare provider)
기간: immediately after vascular access procedure
|
The survey contains 5 items and utilizes a 5-point Likert agreement scale with a score of 1 meaning "completely disagree" and 5 meaning "completely agree." |
immediately after vascular access procedure
|
|
Self formulated procedural satisfaction survey (Patient and Parent)
기간: immediately after vascular access procedure
|
The survey contains 10 items and utilizes a 5-point Likert agreement scale with a score of 1 meaning "completely disagree" and 5 meaning "completely agree." |
immediately after vascular access procedure
|
공동 작업자 및 조사자
수사관
- 연구 책임자: Thomas Caruso, MD,PhD, Stanford University
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .