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Time Together: A Multi-site Nursing Intervention Project Using a Single System Experimental Design (TT)

2017년 10월 24일 업데이트: Umeå University

The aim of this project is to test and evaluate a nursing intervention, Time Together (TT), created to enable quality interactions between patients and staff in psychiatric inpatient care. The research questions are:

Does TT influence the quality of interactions between staff and patients? Does TT influence patients' levels of anxiety and depressive symptoms? Does TT influence staffs' levels of perceived stress and levels of stress of conscience? Does TT influence the prevalence of coercive measures, mean length of hospital stay and the use of PRN medication?

In parallel, a process evaluation will be conducted, answering questions such as:

How do staff and patients describe their experiences of the intervention and how do contextual factors influence the effects of the intervention? What are the relationship between the outcome variables and the degree of compliance with the intended intervention? What problems are there with recruitment and dropouts?

연구 개요

상태

알려지지 않은

개입 / 치료

상세 설명

BACKGROUND:

Despite the long known significance of the nurse-patient relationship, research in psychiatric inpatient care still reports on unfulfilled expectations of, and difficulties in interactions and relationships between patients and staff. As one solution to the contemporary circumstances, interventions that creates structures that allow quality interactions between patients and staff are needed.

INTERVENTION TT is an intervention, developed from the intervention Protected Engagement Time. The structure of TT is that staff, for a fixed time during the day, dedicates their time to exclusively engage with the patients. Other duties of more administrative nature, visits and meetings are organized to be performed at other times during the day. This structure will be tested at three psychiatric inpatient care wards in the north of Sweden.

DESIGN AND METHODS An experimental single system design (A-B-Follow-up) will be used. As TT will be introduced as a routine ward activity during the B phase, all patients and staff on the participating wards will be participating in TT. However, participating in the evaluation will be voluntary. Data will be collected through questionnaires once every seventh weekday during 5 weeks for the A phase, and 12 weeks during B phase.

In parallel, a process evaluation will be conducted using semi structured interviews and participating observations.

연구 유형

중재적

등록 (예상)

3

단계

  • 해당 없음

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion criteria for patients:

  • 18 years or older
  • Admitted to the wards during either A phase, B phase and/or follow-up
  • Experience of at least one TT session is required to participate in the B phase

Exclusion criteria for patients:

- Does not master the Swedish language well enough to complete questionnaires and participate in interviews.

Inclusion criteria for staff:

- Regularly employed at the ward during A and B phase and/or follow-up.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 건강 서비스 연구
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Time Together
Time Together as described under "Interventions"
For a fixed time during the day, staff dedicates their time to exclusively engage with the patients. Different activities will be offered to both patients and staff, such as playing board games, taking a walk, or having individual conversations. Other duties of more administrative nature, visits and meetings will be performed at other times during the day. Through this, opportunities for interaction are both created and protected.
다른 이름들:
  • Protected Engagement Time

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Quality of interactions [patients]
기간: Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
This is measured using The Caring Professional Scale (CPS) that consists of 14 items answered on a 5-point Likert scale.
Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
Perceived stress [staff]
기간: Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
PSS consists of 10 items answered on a 5-point Likert scale
Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)

2차 결과 측정

결과 측정
측정값 설명
기간
Global quality of interactions [patients, staff]
기간: Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
A 100 mm Visual Analogue Scale expressing the most positive and the most negative rating will be anchored at each end
Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
Anxiety and depressive symptoms [patients]
기간: Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
The Hospital Anxiety and Depression Scale (HAD) will be used to measure anxiety and depressive symptoms. All items are scored on a 4-point scale.
Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
Stress of Conscience [staff]
기간: Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
The Stress of Conscience Questionnaire (SCQ) will be used to measure the frequencies of stressful situations and the degree to which these lead to stress of conscience among staff.
Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
Quality of care [staff]
기간: Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
The Quality in Psychiatric Care- Inpatient Staff (QPC-IPS) questionnaire will be used to measure quality of care.
Changes during baseline and intervention period (measured every seventh week day for a total of 16 weeks)
Number of PRN medications given
기간: Changes during baseline and intervention period (measured weekly for a total of 16 weeks)
Data will be retrieved from ward registers.
Changes during baseline and intervention period (measured weekly for a total of 16 weeks)
Length of hospital stay
기간: Changes during baseline and intervention period (measured weekly for a total of 16 weeks)
Data will be retrieved from ward registers.
Changes during baseline and intervention period (measured weekly for a total of 16 weeks)
Use of coercion and violent situations
기간: Changes during baseline and intervention period (measured weekly for a total of 16 weeks)
Data will be retrieved from ward registers.
Changes during baseline and intervention period (measured weekly for a total of 16 weeks)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2017년 1월 1일

기본 완료 (실제)

2017년 6월 1일

연구 완료 (예상)

2017년 11월 1일

연구 등록 날짜

최초 제출

2016년 12월 1일

QC 기준을 충족하는 최초 제출

2016년 12월 1일

처음 게시됨 (추정)

2016년 12월 5일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 10월 26일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 10월 24일

마지막으로 확인됨

2016년 11월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 350000210

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