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Promoting Overall Care and Management Related to Tuberculosis Infection Through Pharmaceutical Care and Text Messaging

Primary Purpose

Pulmonary TB

Status
Unknown status
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
New management mode
Sponsored by
Farman Ullah Khan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Pulmonary TB

Eligibility Criteria

18 Years - 78 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women
  • Newly bacteriologically confirmed TB case (less than a month since diagnosis). This restriction (not more than one-month treatment) does not refer to patients whose most recent treatment outcome was a failure and who were assigned to a new treatment regimen.
  • Own a mobile phone which operates on a telecom provider supported by our SMS platform
  • Know how to and are able to receive SMS messages or Phone Call (Caretaker want to participate in case original patient do not participate)
  • An address or residence location that is readily accessible for visiting, and willingness to inform the study team of any change of address during the treatment and follow-up period.
  • No plans to move out of the catchment areas of the participating TB program sites within 9 months of enrollment.
  • Facilities must have at least one TB doctor and one TB nurse available within the facility.
  • Willingness to comply with study procedures and provide written informed consent prior to study enrollment.

Exclusion Criteria:

  • Diagnosis is extra-pulmonary TB
  • Currently enrolled in a clinical trial that prohibits enrollment in another study. Patients are leaving the area within the next six months.
  • Patients are known at the start of treatment to require the treatment longer than it is recommended TB Management Guidelines for the appropriate type of TB.
  • Previous history of TB, multidrug-resistant (MDR) or extensively drug-resistant (XDR) TB.
  • Very ill patient's cognitive or physical disability that prevents full participation in the study such as vision, hearing, physically challenged, inability to swallow medications and unconscious Unable to answer questions.
  • Pregnant females (treatment of TB infection will be deferred)
  • Patients who are receiving treatment from private clinics (Who are not registered in the government TB sectors and they seek are form private health care facilities.

Sites / Locations

  • National TB Control ProgramRecruiting
  • Pakistan Institute of Medical Sciences Islamabad

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention Group

No Intervention Group.

Arm Description

New management mode intervention: Pharmaceutical care A more recent strategy is pharmaceutical care, where a hospital provides timely patient education, monitoring and management of adverse drug reactions, identifying other drug-related problems, and an evaluation of treatment adherence by a clinical pharmacist. At the first visit, the clinical pharmacist provides a mobile phone number and encourages patients to contact them anytime if they need any consultation on the TB treatment. Short Message Service and Phone calls daily use of the mobile phone for a TB treatment will support pharmaceutical care. TB patients or family members will receive phone calls every evening (except Sunday) during the whole ambulatory TB treatment phase to assure that the patient takes the medication prescribed and provided by the TB physician and to collect information on treatment adherence and possible side effects.

Treatment Group included in the control arm will receive traditional - clinical Directly Observed Therapy (DOT) as recommended by World Health Organization and routine treatment group (6 months treatment regimen); Routine health education provided by health care professionals.

Outcomes

Primary Outcome Measures

TB treatment success rates
TB treatment success rates defined by the World Health Organization. The investigators will compare clinically reported treatment outcomes between the intervention and control groups.
Lost to follow-up among adult drug-sensitive tuberculosis patients.
Lost to follow-up is defined as the difference between the two interventions arms in the proportion of patients who did not start treatment after diagnosis or whose treatment was interrupted for 2 consecutive months or more.
Patient satisfaction questionnaire (usually after treatment time period or 6 to 12 months).
Through Questionnaire before and at the end of treatment from both groups
Quality of life of TB patients
At baseline and upon completion of the treatment initial phase and after starting the continuous phase of the treatment Quality of life of TB patients will be measured by surveys.Whether the disease-specific patient quality of life scores improved in investigational arm patients from baseline to successful completion of treatment By using pre and post data of quality of life questionnaire
The Knowledge, Attitude and Practices (KAP) of the patients about tuberculosis
A Knowledge, Attitude and Practices (KAP) survey is a quantitative method (predefined questions formatted in standardized questionnaires) that provides access to quantitative and qualitative information.The KAP of the patients about tuberculosis will be compared at the end of the intervention in the two groups on basis of information about TB prevention and treatment.

Secondary Outcome Measures

Adherence to treatment among drug-sensitive tuberculosis patients self reported and clinical record will checked for the follow up visits and drug taken
Adherence [ Time Frame: Assessed daily from date of randomization until the date of a documented treatment outcome, up to 24 months after study enrollment date.Counting the number of administered pills, adequate adherence is more than 80% of administered pills.
The patient-level percentage of total doses
Each patient based on the total number of doses missed out of the total possible number of doses), measured using treatment adherence records reported by triangulated by pill count after 6 months.
Patient satisfaction questionnaire
Perceptions and opinions (if the intervention was helpful, non-helpful, effectiveness) in the intervention arm will be assessed after the study follow-up through a questionnaire of a subset of enrolled individuals at the completion of the participant's treatment.
The proportion of patients improving clinically through questionnaire
Proportion of patients improving clinically (cough, weight gain, night sweats, fever, appetite to compare the treatment completion rates between participants randomized to intervention without intervention with weekly SMS reminders and pharmaceutical care.
Perceptions of Intervention through a questionnaire
Perceptions and opinions (if the intervention was helpful, non-helpful, effectiveness) in the intervention arm will be assessed after the study follow-up through a questionnaire of a subset of enrolled individuals at the completion of the participant's treatment.
Semi-structured interview to check the Feasibility of implementation of the intervention and challenges.
Semi-structured interview with participants to understand challenges, recommendations for improvement. Feasibility of implementation of the intervention and challenges.
To collect patient-specific cost data related to the successfully treated
To collect patient-specific cost data related to the treatment of arms with the intervention.
Psychological Impacts Mental Health Inventory (MHI)-5; well-demonstrated reliability for detecting psychological disorders also mental health screening tool for TB patients will be used
In order to gauge the psychological impacts of the system, the investigators will be looking at participants' perceptions on the likelihood of being cured, how they feel on a given day using the pain scale, and how supported they feel. This data will be collected through questionnaires conducted at each monthly mid-line visit.

Full Information

First Posted
February 6, 2020
Last Updated
November 30, 2020
Sponsor
Farman Ullah Khan
Collaborators
Shaheed Zulfiqar Ali Bhutto Medical University Islamabad Pakistan, Pakistan Institute of Medical Sciences, Quaid i Azam University Islamabad Pakistan
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1. Study Identification

Unique Protocol Identification Number
NCT04264221
Brief Title
Promoting Overall Care and Management Related to Tuberculosis Infection Through Pharmaceutical Care and Text Messaging
Official Title
Randomized Trial of Pharmaceutical Care and Text Messaging Intervention to Improve Tuberculosis Care and Management Among Drug-susceptible Patients in Pakistan.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2020 (Actual)
Primary Completion Date
December 1, 2020 (Anticipated)
Study Completion Date
December 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Farman Ullah Khan
Collaborators
Shaheed Zulfiqar Ali Bhutto Medical University Islamabad Pakistan, Pakistan Institute of Medical Sciences, Quaid i Azam University Islamabad Pakistan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This project aims to standardize the management of "Pharmaceutical care with the two-way text messages and incentive for mobile usage during the treatment for tuberculosis patients, to improve the outcomes and compliance, reduce the risk of transmission and to evaluate the patient perspective in terms of their quality of life, shared decision making and satisfaction with services provided.
Detailed Description
Tuberculosis (TB) remains a top ten leading cause of death globally despite it being a largely curable disease. New effective treatment supervision strategies are needed particularly in low-resource high TB burden settings and a potential solution is in the hands of nearly every patient - a mobile phone. Modern modular design mobile phone software applications ("apps") hold great promise to address this unmet need. Current technologies allow for rapid design modification based on end-user needs, implementation of native operating system (e.g., Android) versions for users with inconsistent internet access, and the integration of the patients' experiences with electronic health records using industry standards. Apps can perform multiple functions (e.g., automated reminders, symptom tracking, secure messaging, and multi-media education). Another strategy is pharmaceutical care which is utilized to enhance TB treatment compliance along with usage of mobile technologies, where clinical pharmacists provide patient education to improve the patient's knowledge on the disease and medication use and address the patient's drug-related problems. The use of a pharmaceutical care model to improve treatment outcomes and enhance adherence is on the rise in healthcare organizations. At the first visit, the clinical pharmacist provides a mobile phone number and encourages patients to contact them anytime if they need any consultation on the TB treatment. Patients will make prior arrangements with a study pharmacist to determine a convenient meeting place. These meetings will continue until treatment completion. To our knowledge, worldwide there has only been no randomized controlled trial (RCT) which has described the use of both pharmaceutical care model and two-way Short Message Service (SMS) communication with financial incentives (mobile money transfer cover healthcare costs related to SMS charges) to improve treatment outcomes. To find out both the pharmaceutical care model and two-way SMS communication with financial incentives would be helpful for TB patients in Pakistan. Therefore investigator aimed a study, to find out the effectiveness of trial gauged with the impact of the suggested model on the improved adherence, treatment completion, health-related quality of life and satisfaction with TB care. Investigator will also explore implementation questions regarding acceptability, cost-effectiveness and long-term effects to inform future scale-up in remote areas of Pakistan and other low- and middle-income countries. The functions allow the participant to engage in self-management of their care: self-report daily administration of their TB medication, self-report side effects if applicable, review educational material on TB disease protects other members of the family, encourage treatment, shows complete adherence, increase the relationship between patients and care provider and improves quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary TB

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
None (Open Label)
Masking Description
None (Open Label)
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
New management mode intervention: Pharmaceutical care A more recent strategy is pharmaceutical care, where a hospital provides timely patient education, monitoring and management of adverse drug reactions, identifying other drug-related problems, and an evaluation of treatment adherence by a clinical pharmacist. At the first visit, the clinical pharmacist provides a mobile phone number and encourages patients to contact them anytime if they need any consultation on the TB treatment. Short Message Service and Phone calls daily use of the mobile phone for a TB treatment will support pharmaceutical care. TB patients or family members will receive phone calls every evening (except Sunday) during the whole ambulatory TB treatment phase to assure that the patient takes the medication prescribed and provided by the TB physician and to collect information on treatment adherence and possible side effects.
Arm Title
No Intervention Group.
Arm Type
No Intervention
Arm Description
Treatment Group included in the control arm will receive traditional - clinical Directly Observed Therapy (DOT) as recommended by World Health Organization and routine treatment group (6 months treatment regimen); Routine health education provided by health care professionals.
Intervention Type
Behavioral
Intervention Name(s)
New management mode
Other Intervention Name(s)
Pharmaceutical care, Mobile text, Financial incentive for mobile use
Intervention Description
New management mode intervention: Pharmaceutical care SMS text messages and Phone Calls Behavioural Educational leaflet Self-Administered Therapy A financial incentive for mobile use
Primary Outcome Measure Information:
Title
TB treatment success rates
Description
TB treatment success rates defined by the World Health Organization. The investigators will compare clinically reported treatment outcomes between the intervention and control groups.
Time Frame
24 Months
Title
Lost to follow-up among adult drug-sensitive tuberculosis patients.
Description
Lost to follow-up is defined as the difference between the two interventions arms in the proportion of patients who did not start treatment after diagnosis or whose treatment was interrupted for 2 consecutive months or more.
Time Frame
24 \months
Title
Patient satisfaction questionnaire (usually after treatment time period or 6 to 12 months).
Description
Through Questionnaire before and at the end of treatment from both groups
Time Frame
12 Months
Title
Quality of life of TB patients
Description
At baseline and upon completion of the treatment initial phase and after starting the continuous phase of the treatment Quality of life of TB patients will be measured by surveys.Whether the disease-specific patient quality of life scores improved in investigational arm patients from baseline to successful completion of treatment By using pre and post data of quality of life questionnaire
Time Frame
24 months
Title
The Knowledge, Attitude and Practices (KAP) of the patients about tuberculosis
Description
A Knowledge, Attitude and Practices (KAP) survey is a quantitative method (predefined questions formatted in standardized questionnaires) that provides access to quantitative and qualitative information.The KAP of the patients about tuberculosis will be compared at the end of the intervention in the two groups on basis of information about TB prevention and treatment.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Adherence to treatment among drug-sensitive tuberculosis patients self reported and clinical record will checked for the follow up visits and drug taken
Description
Adherence [ Time Frame: Assessed daily from date of randomization until the date of a documented treatment outcome, up to 24 months after study enrollment date.Counting the number of administered pills, adequate adherence is more than 80% of administered pills.
Time Frame
24 Months
Title
The patient-level percentage of total doses
Description
Each patient based on the total number of doses missed out of the total possible number of doses), measured using treatment adherence records reported by triangulated by pill count after 6 months.
Time Frame
24 Months
Title
Patient satisfaction questionnaire
Description
Perceptions and opinions (if the intervention was helpful, non-helpful, effectiveness) in the intervention arm will be assessed after the study follow-up through a questionnaire of a subset of enrolled individuals at the completion of the participant's treatment.
Time Frame
6-12 months
Title
The proportion of patients improving clinically through questionnaire
Description
Proportion of patients improving clinically (cough, weight gain, night sweats, fever, appetite to compare the treatment completion rates between participants randomized to intervention without intervention with weekly SMS reminders and pharmaceutical care.
Time Frame
24 months
Title
Perceptions of Intervention through a questionnaire
Description
Perceptions and opinions (if the intervention was helpful, non-helpful, effectiveness) in the intervention arm will be assessed after the study follow-up through a questionnaire of a subset of enrolled individuals at the completion of the participant's treatment.
Time Frame
24 months
Title
Semi-structured interview to check the Feasibility of implementation of the intervention and challenges.
Description
Semi-structured interview with participants to understand challenges, recommendations for improvement. Feasibility of implementation of the intervention and challenges.
Time Frame
24 Months
Title
To collect patient-specific cost data related to the successfully treated
Description
To collect patient-specific cost data related to the treatment of arms with the intervention.
Time Frame
24 Months
Title
Psychological Impacts Mental Health Inventory (MHI)-5; well-demonstrated reliability for detecting psychological disorders also mental health screening tool for TB patients will be used
Description
In order to gauge the psychological impacts of the system, the investigators will be looking at participants' perceptions on the likelihood of being cured, how they feel on a given day using the pain scale, and how supported they feel. This data will be collected through questionnaires conducted at each monthly mid-line visit.
Time Frame
6-12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
78 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women Newly bacteriologically confirmed TB case (less than a month since diagnosis). This restriction (not more than one-month treatment) does not refer to patients whose most recent treatment outcome was a failure and who were assigned to a new treatment regimen. Own a mobile phone which operates on a telecom provider supported by our SMS platform Know how to and are able to receive SMS messages or Phone Call (Caretaker want to participate in case original patient do not participate) An address or residence location that is readily accessible for visiting, and willingness to inform the study team of any change of address during the treatment and follow-up period. No plans to move out of the catchment areas of the participating TB program sites within 9 months of enrollment. Facilities must have at least one TB doctor and one TB nurse available within the facility. Willingness to comply with study procedures and provide written informed consent prior to study enrollment. Exclusion Criteria: Diagnosis is extra-pulmonary TB Currently enrolled in a clinical trial that prohibits enrollment in another study. Patients are leaving the area within the next six months. Patients are known at the start of treatment to require the treatment longer than it is recommended TB Management Guidelines for the appropriate type of TB. Previous history of TB, multidrug-resistant (MDR) or extensively drug-resistant (XDR) TB. Very ill patient's cognitive or physical disability that prevents full participation in the study such as vision, hearing, physically challenged, inability to swallow medications and unconscious Unable to answer questions. Pregnant females (treatment of TB infection will be deferred) Patients who are receiving treatment from private clinics (Who are not registered in the government TB sectors and they seek are form private health care facilities.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Farman Ull ah Khan, Phd
Phone
+0092331-9443131
Email
farmankhan@bs.qau.edu.pk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yu Fang, Phd
Organizational Affiliation
Xian Jiaotong University China
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Asim ur Re, Phd
Organizational Affiliation
Quaid i Azam University Islamabad Pakistan
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Farman Ull ah Khan, Phd
Organizational Affiliation
Jiaotong University Islamabad Pakistan
Official's Role
Principal Investigator
Facility Information:
Facility Name
National TB Control Program
City
Islamabad
State/Province
Islammabd
ZIP/Postal Code
46000
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Farman Ull ah Khan
Phone
+92331-3319443131
Email
farmankhan@bs.qau.pk
Facility Name
Pakistan Institute of Medical Sciences Islamabad
City
Islamabad
ZIP/Postal Code
46000
Country
Pakistan
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

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Promoting Overall Care and Management Related to Tuberculosis Infection Through Pharmaceutical Care and Text Messaging

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