Adherence, Patient, Coping Skills, Psychological
Conditions
Brief summary
Using a prospective qualitative approach, explore whether pathologist intervention is feasible as part of multimodal multidisciplinary care model for transplant patients in effecting psychological dimensions such as experience, satisfaction, or patient's understanding of their disease. Additionally, to examine if this intervention improves medication adherence.
Detailed description
Specific Aims 1. Create post-transplant pathologist-led intervention Objective 1a: Recruit 10 patients who have undergone lung transplantation primarily for chronic obstructive pulmonary disease (COPD). Use pathologist to show gross/microscopic explanted organs. Specific Aim 2. Assess the efficacy of intervention pilot Objective 2a: Immediate (within 1 day after pathologist intervention) phone interview to access patient's reaction, feelings, and experience with intervention and understanding of disease. Objective 2b: 1 month later, phone interview asking questions related to medication adherence, patient experience with intervention and lung transplant overall, and patient understanding of disease. Results will be compared to first interview. Objective 2c: Analyze Client Satisfaction Questionnaire (CSQ-8) for quality of life, Basel assessment of adherence to immunosuppressive medications scale (BAASIS) as a self report adherence measure, and conduct a mixed methods/grounded theory analysis of qualitative data (patient experience, disease understanding). This analysis will systematically identify themes, and assign these descriptive words. Specific Aim 3: Finalize intervention protocol based on pilot testing. Objective 3a. Adjust and refine the content and process of intervention protocol based on findings of pilot study Objective 3b. Final changes will assure readiness for large scale study.
Interventions
BEHAVIORALPathologist intervention
viewing explanted organ and microscopy
Sponsors
University of Pittsburgh
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Intervention model description
Prospective, no blinding or randomization
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Lung transplant patient, transplanted after IRB approval of study -Transplanted primarily for COPD * English speaking * within three months of initial transplant (prior to initial discharge) * \> 18 years old
Exclusion criteria
* Transplant indication other than COPD * \<18 year old * Non English speaking
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Basel Assessment of Adherence to Immunosuppressive Medication Scale (BAASIS©) | one day after intervention and assessment for change one month later | The Basel Assessment of Adherence to Immunosuppressive Medication Scale (BAASIS©) was developed to assess adherence to immunosuppressive drugs in adult and adolescent transplant recipients. Initiation starts when a patient takes his/her first dose of medication. This is a binary event (yes/no). Implementation of the dosing regimen refers to the extent to which a patient's actual dosing corresponds to the prescribed dosing regimen, from initiation until the last dose is taken and implies a dosing history. Discontinuation refers to the moment that the patient discontinues his/her medication regimen and is assessed as a time to event. Persistence is thus the duration between time of initiation and the moment the last dose is taken. Any yes response demonstrates issues with medication adherence. |
| Client Satisfaction Questionnaire (CSQ-8) | one day after intervention and assessment for change one month later | The Client Satisfaction Questionnaire is an 8 item measure of client satisfaction. An overall score is calculated by summing the respondent's rating (item rating) score for each scale item. Scores therefore range from 8 to 32, with higher values indicating higher satisfaction. with services with both a parent intervention versus averages of lung transplant patients. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Patient understanding | one day after intervention and assessment for change one month later | Assess if patient has gained more understanding of their condition. No specific scale used, assessed by interview. |
| Patient experience | one day after intervention and assessment for change one month later | Discussing patient's overall experience. No specific scale used, assessed by interview. |
Countries
United States
Outcome results
None listed