The Effect of Telephone Follow-up and Training on Treatment Adherence in Tuberculosis Patients and Contacts (Tuberculosis)
Primary Purpose
Tuberculosis
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Treatment adherence
Sponsored by
About this trial
This is an interventional supportive care trial for Tuberculosis focused on measuring nursing education, tuberculosis, tuberculosis contact, treatment adherence, telephonefollow-up
Eligibility Criteria
Inclusion Criteria:
- With pulmonary TB
- Being voluntary to participate in the study
- Being at and over the age of 18
- Having no communication problems
- Being able to use mobile telephone
Exclusion Criteria:
- Being under 18 years old
- Not voluntary to participate in the study
- Having multi drug resistance
Sites / Locations
- Gaziantep University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Adherence
Standart care
Arm Description
Participants received training, telefollow-up and daily text messages for 6 months.
The standard follow-up applied in the dispensary for this group was performed.
Outcomes
Primary Outcome Measures
Change in treatment adherence during the Follow-up
Tuberculosis Adherence Determination Questionnaire (TADQ) was conducted. It is a 5-point likert scale and minimum and maximum scores of the scale are 26 and 175 and high score signifies that adherence increases.
Secondary Outcome Measures
Full Information
NCT ID
NCT05202431
First Posted
December 14, 2021
Last Updated
January 20, 2022
Sponsor
Tuberculosis Network European Trialsgroup
1. Study Identification
Unique Protocol Identification Number
NCT05202431
Brief Title
The Effect of Telephone Follow-up and Training on Treatment Adherence in Tuberculosis Patients and Contacts
Acronym
Tuberculosis
Official Title
The Effect of Telephone Follow-up and Training on Treatment Adherence in Tuberculosis Patients and Contacts: A Randomised, Controlled and Quasi Experimental Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
July 30, 2019 (Actual)
Study Completion Date
July 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tuberculosis Network European Trialsgroup
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Tuberculosis (TB) is a preventable and curable disease mostly affecting lungs and caused by the bacteria called as Mycobacterium Tuberculosis (MTB). It is estimated that approximately 10 million people are diagnosed with TB every year in the world and 1.7 billion people are infected by MTB and at risk in terms of the development of the disease. Contacted person is the one who shares the same environment with the patient suffering from contagious TB and is exposed to MTB bacilli.
Today, the aim of the TB control and prevention programs is to determine the active TB patients and provide cure by healing and also to screen those contacted with the TB patients and determine whether or not they have latent TB infection and treat them and to detect the active cases among the contacts. In the current guidelines, the importance of screening all the contacts of the patients with pulmonary TB and applying a protective treatment for the household in terms of community health care is emphasised. For this reason, it is of prime importance to perform contact screening of the relatives of the TB patients and apply protective treatment. The patients receiving TB and TB protection treatment need to use medicine regularly for at least six months. It is highly important to adherence this period for the success of the treatment. However, it has been reported in the literature that the rate of nonadherence to the TB treatment varies between 20-80% and the nonadherence to the TB treatment is the most serious barrier in the control of the disease. İncomplete treatment may result in long-lasting infection, drug resistance, relapse, and death.
In the litareture, it has been stated in the study conducted with the individuals with some chronic diseases that tele-follow-up is effective in providing the self-care agency of patients and the cognitive-social adaptation. It has been reported that some problems emerge especially in the TB patients such as the interruption of treatment, forgetting medication (24.5%), side-effects of drugs, (23.3%), symptomatic recovery (19.5%), failure to know the necessity of completing the life cycle of drugs by most of patients and not receiving adequate training and these problems may be managed more effectively by tele-follow-up.
As is known, nurses are involved in all the processes of protecting-promoting the health of the individuals, families and society and their recovery in case of disease. Moreover, providing the protective treatment by performing the required screening for treating TB patients, their follow-up and preventing the development of disease in contacted ones has a vital importance in preventing the spread of TB in the society. Nurses may follow the findings of patients, obtain information about the process, produce information and transmit information with this system (reporting drug changes, performing training follow-up of patients etc.). In the literature, it has been emphasised that tele-mobile nursing services is a cost-effective method since it decreases the hospitalisation rate and period of the TB patients. Accordingly, the main aim of this study is to assess the effect of the training and the telephone follow-up provided by the nurse for the TB patients and contacts on the medication adherence.
Detailed Description
This research was conducted as a randomised, controlled and quasi-experimental study to determine the effect of the training and telephone follow-up provided to the TB patients and contacts on the treatment adherence. The population of the study was composed of the patients receiving treatment in a tuberculosis control dispensary between July 2018-July 2019. The sample size was calculated to be 28 in each group through power analysis. Eighty-one TB patients and 90 TB contacts were included in the study. However, 15 TB patients and 3 contacts were excluded since they were transferred to another dispensary and they died. The study was completed with 66 TB patients in the intervention (n= 32) and control groups (n=34) and 87 contacts in the intervention (n= 41) and control groups (n = 46) The TB patients who applied to the dispensary and their contacts were informed about the aim and scope of the study. Then, four groups were formed by using the randomisation menu of the computer program: the intervention and control groups for the TB patients and the intervention and control groups for the contacts. The randomisation was conducted by a statistics specialist who had no contact with the participants. All participants were blinded to the randomisation procedure. However, the researchers were not blinded to the patient groups, due to the nature of the intervention.
The interviews were performed by using the face-to-face interview technique in the outpatient clinic. In the first interview, the questionnaire was applied to four groups; TB intervention and TB control group, Contact intervention and Contact control group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
nursing education, tuberculosis, tuberculosis contact, treatment adherence, telephonefollow-up
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Adherence
Arm Type
Experimental
Arm Description
Participants received training, telefollow-up and daily text messages for 6 months.
Arm Title
Standart care
Arm Type
No Intervention
Arm Description
The standard follow-up applied in the dispensary for this group was performed.
Intervention Type
Behavioral
Intervention Name(s)
Treatment adherence
Intervention Description
The patients were reminded to take drug by patient training, telephone follow-up, and daily sms. It was determined that the effect of the training and telephone follow-up provided to the TB patients and contacts on the treatment adherence.
Primary Outcome Measure Information:
Title
Change in treatment adherence during the Follow-up
Description
Tuberculosis Adherence Determination Questionnaire (TADQ) was conducted. It is a 5-point likert scale and minimum and maximum scores of the scale are 26 and 175 and high score signifies that adherence increases.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
With pulmonary TB
Being voluntary to participate in the study
Being at and over the age of 18
Having no communication problems
Being able to use mobile telephone
Exclusion Criteria:
Being under 18 years old
Not voluntary to participate in the study
Having multi drug resistance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sema Aytac
Organizational Affiliation
Gaziantep
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gaziantep University
City
Gaziantep
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Effect of Telephone Follow-up and Training on Treatment Adherence in Tuberculosis Patients and Contacts
We'll reach out to this number within 24 hrs