The Impact of Mindfulness-Based Intervention on Pro-Inflammatory Cytokines

Sponsor
Jordan University of Science and Technology (Other)
Overall Status
Completed
CT.gov ID
NCT06064708
Collaborator
(none)
64
2
2
4.7
32
6.9

Study Details

Study Description

Brief Summary

Background: Hemodialysis is considered as an effective therapy to remove harmful wastes from the body and to improve the quality of life in patients suffering from end-stage renal disease (ESRD). However, patients who receive hemodialysis perceive various stressors that are harmful to their physical and psychological well-being, particularly the immune system. Therefore, it is necessary to implement effective and practical therapeutic strategies to enhance the quality of life in this population. Mindfulness-based intervention is an effective mind-body connection program that is inadequately used in patients undergoing hemodialysis.

Objective: The current study aimed to investigate the effect of mindfulness-based intervention on physical and psychological symptoms (e.g., stress, anxiety, and depression) and pro-inflammatory biomarker levels (e.g., TNF, interleukin-6, and C-reactive protein) in patients with ESRD undergoing hemodialysis.

Method: Repeated measures, randomized, control experimental design was used. A convenience non-probability sampling technique to select the sample from the hemodialysis unit in the Princess Haya Bint AL_Hussine Hospital. The participants who were eligible and agreed to participate were randomly distributed into experimental (n = 31) and control (n = 30) groups. During their hemodialysis sessions, the experimental group' participants practiced 30-minute mindfulness-based intervention; three times a week for eight weeks). The Mindful Attention Awareness Scale (MAAS), Depression, Anxiety, and Stress Scale - 21 (DASS-21), Patient Health Questionnaire (PHQ-15), and serum blood levels (for tumor necrosis factor, interleukin-6, and C-reactive protein) were used to measure the dependent variables for both groups at baseline, after five weeks of the intervention, and at its end (eight weeks).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness-based intervention
N/A

Detailed Description

Background

Hemodialysis is considered as an effective and essential therapy to remove harmful wastes from the body and to improve the quality of life (QoL) of end-stage renal disease (ESRD) patients. However, patients undergoing hemodialysis experience multiple stressors (Finnegan-John & Thomas, 2013), negatively affecting their psychological and physical health, especially in relation to the immune system (Black & Slavich, 2016). Previous studies have indicated that patients undergoing maintenance hemodialysis experience a variety of physical and psychological symptoms (i.e., anxiety, fatigue, muscular spasms, and joint and bone pain), caused by a combination of stress, the disease itself, and intensive treatment (Hackett & Jardine, 2017; Hintistan, & Deniz, 2018), which has diverse effects including increased suicidal ideation (Yavuz, et al., 2022), impaired physical activity (Mallamaci et al., 2020), reduced QoL (Vasilopoulou et al., 2016), increased susceptibility to infectious disease (Maydych, 2019), and increased mortality and morbidity (Lv & Zhang, 2019).

High levels of blood proinflammatory markers, including C-reactive protein (CRP), tumor necrosis factor alpha (TNF-α), and interleukine-6 (IL-6), have been found in the majority of patients with ESRD (Abdel-Messeih et al., 2020; Park et al., 2022). The aetiology of inflammation in patients with ESRD is multidimensional, including patient-related causes, such as ESRD-related symptoms, comorbidity, and hemodialysis-related issues, especially those relating to the biocompatibility and quality of the dialysate and the dialysis membrane. These high levels of proinflammatory biomarkers in ESRDPs have been found to cause injury to other bodily organs in addition to the kidney, increasing morbidity and mortality (Abdel-Messeih et al., 2020).

Mind-body connection strategies such as mindfulness-based interventions (MBIs) are purposefully adopted in a wide range of structured interventions and have been proven to be highly effective in treating many physical and psychological symptoms of a wide range of psychiatric conditions associated with diverse chronic illnesses (Chu et al., 2021). MBIs reinforce adaptive coping processes and enhance positive reappraisal (Aliche & Onyishi, 2020). They enhance coping, reduce stress, improve mood and enhance the quality of spirituality and personal development in the adaptation of ESRD diagnosis and treatment (Sohn et al., 2018). They can also aid patients to be less reactive and to deal with fluctuating feelings through learning to accept the current experience more effectively, which ultimately reduces physical and emotional stress reactions (Chin-Lun Hung, 2019). Stress and emotional reactions are associated with increased levels of proinflammatory markers, whereby MBI could be effective in decreasing such markers by reducing stress and emotional reactions.

Many studies have demonstrated that MBI can improve psychophysical symptoms (i.e., stress, anxiety, depression, sleep disturbances, and pain) and pro-inflammatory markers (i.e., CRP, IL-6, and TNF α) in different psychiatric and medical populations (Aliche & Onyishi, 2020; Black & Slavich, 2016; Chu et al., 2021). A few studies have examined MBI's effects on limited numbers of psychophysical symptoms in ESRD patients undergoing hemodialysis, but they were hampered by severe limitations, such as small sample sizes and unstandardized intervention protocols.

For example, five weekly sessions of MBI improved perceived stress and QoL through the development of emotional regulation in patients undergoing hemodialysis (Alhawatmeh et al., 2022). Evidence has also shown that the practice of MBI reduced sleep disturbances, anxiety, stress, and depression in such patients (Alhawatmeh et al., 2022; Hackett & Jardine, 2017; Nejad et al., 2018). An extensive literature search did not find any previous study that examined the impact of MBI on serum proinflammatory biomarkers in patients with ESRD undergoing hemodialysis, although such interventions reduced proinflammatory markers such as CRP, interleukin-6 and TNF in different clinical conditions such as cancer, rheumatoid arthritis, and ulcerative colitis (Black & Slavich, 2016). Thus, the goal of this research is to investigate the effect of MBI on physical and psychological symptoms (e.g., stress, anxiety and depression) and proinflammatory biomarkers (e.g., TNF and CRP) in patients with ESRD undergoing hemodialysis.

Methodology

Design

A randomized, wait-list, control trial with two groups, and repeated measurement (RM) design was used in this randomized controlled trial (RCT).

Setting and Sample

The study was carried out in a military hospital located the Northern Jordan. It serves all patients, regardless of whether they have private, military, or public insurance. The hospital includes a dialysis unit with 30 dialysis machine beds and 112 patients are treated on average each week.

The inclusion criteria included patients with ESRD who: underwent hemodialysis thrice weekly, were at least 18 years old, were capable of reading and writing in Arabic, and agreed to participate. Patients under total parenteral nutrition (TPN), undergoing psychotherapy, taking psychopharmacological or anti-inflammatory drugs, and having immunocompromised and infectious illnesses were excluded from the research. Convenience sampling initially recruited 64 participants, who were then randomly assigned by a researcher who was not involved in the patient assessment or recruitment process to the experimental (n=32) or control groups (n=32), using a simple 1:1 computer-generated sequence. However, 61 patients completed the study with 31 in the experimental group and 30 patients in the control group.

Determination of Sample Size

G*power 3.1.9.4 was used to calculate the sample size. Given a mixed-design repeated measures analysis of variance (ANOVA) (among groups and between groups), effect size of 0.25 and Cronbach's alpha coefficient of 0.05, and a power of 0.95, the recommended sample size is 44 patients. Taking into consideration a non-response and attrition rate of approximately 45%, as reported in a similar study (Alhawatmeh et al., 2022), the final required sample size was determined to be approximately 64 patients.

Data Collection Instruments

The data were collected three times (at baseline, after five weeks, and at the end of the intervention) using ELIZA based-biological blood tests for pro-inflammatory biomarkers and an Arabic self-reported questionnaire comprising four parts: (1) demographic and behavioral characteristics, (2) The Mindful Attention Awareness Scale (MAAS-15) (Rayan & Ahmad, 2018), (3) the Depression, Anxiety and Stress Scale (DASS-21) (Al-Dwaikat et al., 2021), and (4) the Patient Health Questionnaire (PHQ-15) (AlHadi et al., 2017).

Demographic and behavioral characteristics

Age, gender, religion, nationality, smoking status, comorbidities, daily sleep and exercise hours, general health, nutritional status, and coping ability were all included in this section of the questionnaire. Three questions were used to evaluate general health status ("How would you generally rate your overall health?"), nutritional status ("In general, how would you generally rate your nutritional status?"), and coping ability ("How would you generally rate your coping skills?"). Responses were graded using a five-point Likert scale, with responses ranging from 1 ("poor") to 5 ("excellent") (Alhawatmeh et al., 2022).

Intervention

The experimental group received 30 minutes of MBI according to Smith's (2005) MBI protocol, which is a standardized theory-based intervention. It was administered during guided chairside interventions during participants' hemodialysis sessions, three times a week over eight weeks (comprising 720 minutes in total).This approach has been demonstrated to be viable and effective for patients undergoing hemodialysis (Alhawatmeh et al., 2022; Thomas et al., 2017).

Smith's (2005) MBI protocol comprises six components:
  1. Being mindful of the breath, by taking deep breath and simply exhaling with bay attention to airflow (5 minutes).

  2. Being mindful of the body, by attending to how the body senses from head to toe noting any sensation (5 minutes).

  3. Being mindful of the thought, by attending to the mind as thoughts and ideas come and go, noticing it, letting it go, and continue attending to the mind repeatedly (5 minutes)

  4. Being mindful of the sound, by attending to sounds without judging about them, noticing them, letting them go, and continuing waiting. (5 minutes)

  5. Being mindful during walking, by imagining walking in a free path Without thinking about where to go, just imagining every step location (5 minutes)

  6. Full meditation, by opening one's eye and living mindful of the world of the moment, when noting something (sound, thought, sensation…) the individual must let it go and wait for what comes next (5 minutes).

Participants in the experimental group received records that provide program instructions via WhatsApp and e-mail (iOS and Android), to ensure the consistent delivery of the intervention. The Foundation Course (2 hours) was conducted by experienced researchers who taught the participants in the experimental group the basics of the MBI program. To ensure that they could practice effectively after they received appropriate training, they were supervised by the researchers during the intervention sessions. During the eight weeks and at bedtime at night, the participants were optionally advised to commit to practicing a mind-body connection program at home.

The principal investigator (PI) received a four-day training session on "Mind-Body Practice". A checklist was maintained by the PI containing all steps of the intervention (each step and the length of time to spend on each step) to achieve high levels of adherence. The intervention benefits of the investigation were not determined for participants to prevent bias, and the participants were asked not to use any psychiatric or alternative medicine treatments to enhance sleep or mood, and to notify the researcher of any problems or concerns if needed. Also, patients' electrical medical records were checked regularly during the intervention to ensure they did not receive any anti-inflammatory or psychological medication, and that they were not suffering from any infectious diseases. Any potential interruption (e.g., the dialysis machine alarm) was managed immediately by the attending healthcare professionals.

The control group only received usual care, comprising biomedical normative dialysis treatment (the participants in this group did not receive any kind of additional treatment or holistic components). However, upon completion of the study, audio recordings of the intervention protocol were provided and explained to participants in the control group.

Procedure

After obtaining the IRB approval, the hospital managers were contacted by the study researcher to get approval for the study. After obtaining approval, the patients were contacted in person to describe the purpose of the study. Patients who decided to participate were asked to sign the consent form. After that, baseline measurements were taken in the hemodialysis unit in private contexts, where nobody else was present while participants filled out the questionnaire. A research assistant who did not participate in the other study phases collected the data, including blood sampling. This research assistant, who was an experienced registered nurse working in the hemodialysis unit for 10 years, followed strict infection control protocol during blood sampling.

After that, the participants were randomly distributed into the experimental and control groups according to a straightforward 1:1 computer-generated sequence, giving them an equal chance of being in either of the two groups. The foundation course was then conducted for the experimental group.

The MBI was delivered at the hospital, as described previously, and the participants in the experimental group were optionally advised to commit to practicing the study intervention program at home. Participants in both groups had to practice their normal routines of life before the study and not take psychiatric or alternative treatments to improve mood and notify the researcher if necessary.

Following baseline (Time 1), data was collected for the second and third time five and eight weeks after initiating the intervention (Time 2 and Time 3, respectively). All measurements were privately taken in similar situations and environments in the hemodialysis unit by the research assistant who took the baseline measurements. Nobody was present when participants filled out the questionnaire.

Data Analysis

SPSS version 25 was used to analyze the data. Descriptive statistics frequency, mean, and standard deviation were used as appropriate to describe the study participants. Repeated-measure ANOVA (RM ANOVA) (within-between-subject design) was used to test the study hypotheses. To assess whether there were significant mean differences between the study groups at each time measure and between the three-time measurements within each group, independent t-tests and repeated-measure ANOVA (between-subject only) respectively were conducted as post hoc testing.

Ethical Considerations

Jordan University of Science and Technology's Institutional Review Board (IRB) approved the proposed study. Participants who agreed to participate in the study were asked to sign a consent form that described the purpose and scope of the research. They confirmed that they had the freedom to reject participation in the study and that such rejection would not affect the care they received. They were assured that the research data would be stored in a secure location in a locked cabinet accessible only to the researcher, with numbers replacing their names to avoid their personal identification. No patients were excluded from the trial because of their gender, race, or nationality. During the intervention, if any patient felt dizzy or uncomfortable, the intervention was stopped, and the attending physician was informed immediately.

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
the participants were randomly distributed into the experimental and control groups according to a straightforward 1:1 computer-generated sequence, giving them an equal chance of being in either of the two groups.the participants were randomly distributed into the experimental and control groups according to a straightforward 1:1 computer-generated sequence, giving them an equal chance of being in either of the two groups.
Masking:
Single (Investigator)
Masking Description:
A research assistant who did not participate in the other study phases collected the data, including blood sampling.
Primary Purpose:
Supportive Care
Official Title:
The Impact of Mindfulness-Based Intervention on Psychosomatic Symptoms and Pro-Inflammatory Cytokines in Patients Undergoing Hemodialysis: An Experimental Study
Actual Study Start Date :
Apr 10, 2023
Actual Primary Completion Date :
Aug 10, 2023
Actual Study Completion Date :
Aug 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients with ESRD receiving mindfulness-based intervention

Patients with ESRD who received mindfulness-based intervention: underwent hemodialysis thrice weekly, were at least 18 years old, were capable of reading and writing in Arabic, and agreed to participate. Patients under total parenteral nutrition (TPN), undergoing psychotherapy, taking psychopharmacological or anti-inflammatory drugs, and having immunocompromised and infectious illnesses were excluded from the research.

Behavioral: Mindfulness-based intervention
The experimental group received 30 minutes of MBI according to Smith's (2005) MBI protocol, which is a standardized theory-based intervention. Smith's (2005) MBI protocol comprises six components: Being mindful of the breath (5 minutes). Being mindful of the body (5 minutes). Being mindful of the thought (5 minutes) Being mindful of the sound (5 minutes) Being mindful during walking (5 minutes) Full meditation (5 minutes).

No Intervention: Control group

The control group including patients with ESRD with the inclusion criteria similar to the experimental group received usual care, comprising biomedical normative dialysis treatment (the participants in this group did not receive any kind of additional treatment or holistic components). However, upon completion of the study, audio recordings of the intervention protocol were provided and explained to participants in the control group.

Outcome Measures

Primary Outcome Measures

  1. C-reactive protein [8 weeks]

    Serum CRP: This biomarker was analyzed using the ELISA protocol

  2. Interleukin 6 [8 weeks]

    This biomarker was analyzed using the ELISA protocol

  3. Tumor necrosis factor-alpha [8 weeks]

    This biomarker were analyzed using the ELISA protocol

  4. Trait mindfulness [8 weeks]

    Mindful Attention Awareness Scale (MAAS-15) was used to assess dispositional mindfulness (Brown & Ryan, 2003). The Arabic version of MASS-15 is a valid and reliable scale (Rayan & Ahmad, 2018).

  5. Emotional symptoms [8 weeks]

    Depression, Anxiety and Stress Scale (DASS-21) was used to assess emotional symptoms (Antony et al., 1998). The Arabic version showed valid and reliable results in patients with chronic diseases such as diabetes mellitus (Al-Dwaikat et al., 2021)

  6. Physical symptoms [8 weeks]

    Patient Health Questionnaire (PHQ-15) was used to measures the severity of 15 somatic symptoms (Kroenke et al., 2002). The Arabic PHQ-15 is a valid and reliable scale (AlHadi et al., 2017).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with ESRD who underwent hemodialysis thrice weekly

  • were at least 18 years old

  • were capable of reading and writing in Arabic

  • agreed to participate.

Exclusion Criteria:
  • Patients under total parenteral nutrition (TPN)

  • undergoing psychotherapy

  • taking psychopharmacological or anti-inflammatory drugs

  • having immunocompromised and infectious illnesses

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hossam AlHawatmeh Irbid None Selected Jordan 22110
2 Jordan University of Science and Technology Irbid None Selected Jordan 22110

Sponsors and Collaborators

  • Jordan University of Science and Technology

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hossam Najjem Alhawatmeh, Associate professor, Jordan University of Science and Technology
ClinicalTrials.gov Identifier:
NCT06064708
Other Study ID Numbers:
  • 34/156/2023
First Posted:
Oct 3, 2023
Last Update Posted:
Oct 3, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hossam Najjem Alhawatmeh, Associate professor, Jordan University of Science and Technology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 3, 2023