Psychological Clinical Trial
Official title:
A Brief Hope Intervention to Increase the Hope Level and to Improve the Physical and Mental Health of Patients Receiving Palliative Care: a Randomized Controlled Trial
Aims. This paper describes the study protocol of a manualized brief positive intervention
(BHI). In addition, it reports the on the modification of a hope intervention based on the
theoretical proposition - hope theory, and its feasibility when applying to palliative
cancer and non-cancer patients.
Background. Hope was found to account for therapeutic changes in clients with depressive
symptoms or chronic pain. Nevertheless, little is known about the integration of such active
ingredients to brief and low intensity psycho-therapeutic interventions to patients
receiving palliative care were not adequately tested.
Design. The study included two stages: (1) manual development, and (2) a single blinded
randomized controlled trial.
Methods. Participants will be randomly assigned in equal number into either the brief hope
intervention or the controlled arm on completion of the baseline assessment. Participants of
the intervention group will be receiving the four-week intervention, while those allocated
to the control arm will be receiving the routine care and social chats. The intervention is
a manualized program that consists of four sessions at weekly intervals (two face to face
sessions and two telephone follow up in between). The core content is modified from an eight
sessions hope therapy. Expert panel feedback and trial on targeted populations were
completed. Four participants received the program to determine its acceptability prior to
feasibility testing. The process and practical considerations were evaluated to allow
refinement of the program and to ensure the quality of intervention.
Outcome measures comprise of changes in state hope score and the depression scores measured
respectively by State Hope Scale and Centre for Epidemiological Study Depression Scale. The
secondary outcomes are the common signs and symptoms in cancer patients measured by The
Condensed Memorial Symptom Assessment Scale. Data collection will be done prior to the
intervention (baseline), immediately and one month after the intervention. Additional use of
qualitative interview to explore their experiences in the intervention, including
satisfaction with the intervention and the treatment fidelity will be conducted.
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | May 1, 2018 |
Est. primary completion date | April 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Age = 18 years 2. Clinically diagnosed to have cancer or patients receiving palliative care 3. Willing to participate in face-to-face activities and telephone follow up 4. Alert and oriented, able to sustain for approximately one hour of attention and interaction 5. Communicable in Cantonese, able to read and write Chinese 6. Could be reached by phone Exclusion Criteria: Patients having one or above of the below conditions will be excluded from the study. 1. Patients who have planned operation or further chemotherapy and/or radiotherapy within three months 2. Patients who are unable to communicate in Cantonese 3. Patient who has hearing deficit 4. Patient who are disoriented, delirious or cognitively impaired 5. Patients who have been or is receiving counseling or psychotherapy 6. Patients who are clinically depressed diagnosed by medical doctors |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
The Hong Kong Polytechnic University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Center for Epidemiological Studies Depression Scale (CES-D) | CES-D is a 20-item self-report scale measures the frequency of occurrence of depressed mood within one week is in a response format of 4-point Likert scale. The four options are 'rarely or none of the time' (less than 1 days); "some or a little of the time' (1-2 days), "occasionally or a moderate amount of the time" (3-4 days); and "most or all of the time" (5-7 days). Total scores ranging from 0 to 60, with higher ratings denoting higher frequency of depressive symptoms. | 4 weeks | |
Other | Healthcare Resource Utilization | Hospital readmission rate, emergency room utilization and mortality rate | 3 months | |
Primary | State Hope Scale (SHS) | The SHS is a self-report instrument consisting of 6 items (Snyder et al., 1996) used to assess the two ongoing hope indices related to the pathways and agency of hopeful thinking. For instance, 'I can think of many ways to reach my current goals'. It takes approximately 5 minutes to complete. It is rated on an 8-point scale with 1 = definitely false and 8 = definitely true. | 4 weeks | |
Secondary | The Condensed Memorial Symptom Assessment Scale (CMSAS) | The CMSAS a an abbreviated version of the short form MSAS-SF (Chinese version). The instrument measures 14 prevalent symptoms and comprises of two subscales: (1) Physical Symptom (CMSAS PHYS -11 items), (2) Psychological Symptom (CMSAS PSYCH - 3 items), and total score of the CMSAS (CMSAS SUM). Physical symptoms included lack of energy, lack of appetite, pain, dry mouth, weight loss, feeling drowsy, shortness of breath, constipation, difficulty sleeping, difficulty concentrating, and nausea. The psychological symptoms include worrying, feeling sad, and feeling nervous. The items were scored on a 5-point Likert scale from 0 = not at all to 4 = very much. | 4 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04680611 -
Severe Asthma, MepolizumaB and Affect: SAMBA Study
|
||
Active, not recruiting |
NCT05661799 -
Persistence of Physical Activity in People With Type 2 Diabetes Over Time.
|
N/A | |
Recruiting |
NCT04356924 -
Psychological Treatment to Support the Consequences of Cognitive Impairment
|
N/A | |
Terminated |
NCT04241055 -
Values Affirmation to Improve Teachers' Outcomes
|
N/A | |
Active, not recruiting |
NCT04109677 -
AIM CONTROL and SWECON - Handball The SWEdish CONcussion Study in Elite Handball
|
||
Recruiting |
NCT03624348 -
The Impact of 8 Weeks of a Digital Meditation Application on Work Stress
|
N/A | |
Recruiting |
NCT03706807 -
Effect of the Mindfulness-Based Health Promotion Program (MBHP) in the Elderly: a RCT
|
N/A | |
Recruiting |
NCT05949047 -
Smartphone-based Cognitive Emotion Regulation Training for Unpaid Primary Caregivers of Persons With Alzheimer's Disease
|
N/A | |
Completed |
NCT06010407 -
Examining the Attitudes of Physiotherapists on Patient Psychology
|
||
Not yet recruiting |
NCT05442294 -
"Juego de LLaves": Study Protocol of a Universal School-based Drug Use Prevention Program (PSIDUP)
|
N/A | |
Active, not recruiting |
NCT05419167 -
STEP-COVID: A Program for Pregnant Women During the SARS-CoV-2 Pandemic
|
Phase 1 | |
Completed |
NCT04848948 -
Impact of Calory Restriction and Biofeedback on Endocrine and Mental Health
|
N/A | |
Completed |
NCT05849792 -
Internet-based Physical Activities Randomized Controlled Trial in Mild/Moderate Depression Participants: SONRIE Project
|
N/A | |
Active, not recruiting |
NCT03610594 -
Effects of Kalaripayattu on Psychological Wellbeing and Behavior in Children
|
N/A | |
Completed |
NCT05510414 -
Evaluation of a Psychological Capital Intervention to Alleviate Burnout and Regulate Immunity Among Oncology Nurses
|
N/A | |
Completed |
NCT05149066 -
#KindGirlsInACTion: A Programme for the Promotion of Mental Health of Female Adolescents
|
N/A | |
Completed |
NCT05264792 -
Remote Coaching for Supporting the Implementation of Depression Care in Primary Care in Rural India
|
N/A | |
Enrolling by invitation |
NCT05977894 -
Floatation Experience in Nurses and Physicians
|
||
Recruiting |
NCT05616988 -
Metabolomic Evaluation of Psycho-surgical Synergy on Body Image Restoration After Breast Cancer
|
N/A | |
Completed |
NCT04147741 -
Effects of a Pre-Workout on Performance, Perceptual Responses, Energy Feelings and Muscular Properties, After a Training Microcycle in Adults.
|
N/A |