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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02730078
Other study ID # NMRR- 15-1144-24803
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2016
Est. completion date December 2017

Study information

Verified date July 2019
Source Universiti Putra Malaysia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the clinical trial is to evaluate the effectiveness of a relatively simple and short value-based emotion-focused educational programme in adults with type 2 diabetes (VEMOFIT) on diabetes-related distress, depressive symptoms, illness perception, medication adherence, quality of life, diabetes self-efficacy, self-care and clinical outcomes.


Description:

Type 2 diabetes (T2D) patients experience many psychosocial problems related to their diabetes, as well as social- and work-related relationships. These often lead to emotional disorders such as distress, stress, anxiety and depression. Without proper care, these patients use more often negative coping strategies and more frequently expect that their diabetes will negatively affect their future. A cluster randomised controlled trial will be conducted in 10 public health clinics (HC) in Malaysia. These clusters are eligible if they are providing standard diabetes care according to national clinical practice guidelines, not involved in similar trial and having nurses to be trained to deliver the VEMOFIT educational programmes. Pre-stratification by cluster size and geographic areas of the HCs will get randomised five HCs to the VEMOFIT group (VG) and attention-meetings group (AG), respectively.


Recruitment information / eligibility

Status Completed
Enrollment 124
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Malay patients

- Diagnosed with T2D for at least two years

- On regular follow-up with at least three visits in the past one year

- Have diabetes-related distress (mean DDS-17 score = 3)

- Showing poor disease control (not reaching targets for one of the three biomarkers, namely HbA1c = 8%, blood pressure = 140/90 mmHg and LDL-C > 2.6 mmol/L)

Exclusion Criteria:

- Patients who are enrolled in other clinical studies

- Pregnant or lactating

- Having psychiatric/ psychological disorders that could impair judgments and memory

- Patients who cannot read or understand English or Malay

- Patients who scored = 20 on the Patient Health Questionnaire-9 (PHQ-9) that suggest a severe depression

Study Design


Intervention

Behavioral:
VEMOFIT
The VEMOFIT intervention involves four biweekly two hours sessions over a period of about six weeks, and a booster at three months follow-up. It consists of a mixture of 1) exploring illness perceptions and personal meanings of diabetes, 2) cognition-focused education on diabetes and practical skills in self-management and 3) emotion-focused training on recognising emotions in the self and others. Each group will consist of 10 to 12 participants of equal representation by the patients and their significant others.
Attention-meetings (AG)
Patients in the health clinics randomised to the AG, will receive the usual T2D care by the clinic doctors and education by the clinic paramedics based on the recommendations in the Malaysian clinical guidelines. At T1, T2 and T4, patients (not including their significant others) in AG will be gathered in groups of 10-12 people for the primary and secondary outcomes evaluation. This session will include general discussion on feeling about and coping with T2D, social support at home and satisfaction with treatment and care received at the respective clinics.

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Universiti Putra Malaysia Ministry of Health, Malaysia, UMC Utrecht

References & Publications (7)

Chew BH, Fernandez A, Shariff-Ghazali S. Psychological interventions for behavioral adjustments in diabetes care - a value-based approach to disease control. Psychol Res Behav Manag. 2018 May 4;11:145-155. doi: 10.2147/PRBM.S117224. eCollection 2018. Review. — View Citation

Chew BH, Mukhtar F, Sherina MS, Paimin F, Hassan NH, Jamaludin NK. The reliability and validity of the Malay version 17-item Diabetes Distress Scale. Malays Fam Physician. 2015 Aug 31;10(2):22-35. eCollection 2015. — View Citation

Chew BH, Shariff-Ghazali S, Fernandez A. Psychological aspects of diabetes care: Effecting behavioral change in patients. World J Diabetes. 2014 Dec 15;5(6):796-808. doi: 10.4239/wjd.v5.i6.796. Review. — View Citation

Chew BH, Vos RC, Fernandez A, Shariff Ghazali S, Shamsuddin NH, Ismail M, Rutten GEHM. The effectiveness of an emotion-focused educational programme in reducing diabetes distress in adults with type 2 diabetes mellitus at 12-month follow-up: a cluster ran — View Citation

Chew BH, Vos RC, Metzendorf MI, Scholten RJ, Rutten GE. Psychological interventions for diabetes-related distress in adults with type 2 diabetes mellitus. Cochrane Database Syst Rev. 2017 Sep 27;9:CD011469. doi: 10.1002/14651858.CD011469.pub2. Review. — View Citation

Chew BH, Vos RC, Shariff Ghazali S, Shamsuddin NH, Fernandez A, Mukhtar F, Ismail M, Mohd Ahad A, Sundram NN, Ali SZ, Rutten GE. The effectiveness of a value-based EMOtion-cognition-Focused educatIonal programme to reduce diabetes-related distress in Malay adults with Type 2 diabetes (VEMOFIT): study protocol for a cluster randomised controlled trial. BMC Endocr Disord. 2017 Apr 4;17(1):22. doi: 10.1186/s12902-017-0172-8. — View Citation

Chew BH, Vos RC, Stellato RK, Ismail M, Rutten GEHM. The effectiveness of an emotion-focused educational programme in reducing diabetes distress in adults with Type 2 diabetes mellitus (VEMOFIT): a cluster randomized controlled trial. Diabet Med. 2018 Jun — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Health-care utilisation/hospitalisation Number of visits to healthcare facilities including hospitalisation, patient's record and diary used in the study 6-month [T2]
Other Health-care utilisation/hospitalisation Number of visits to healthcare facilities including hospitalisation, patient's record and diary used in the study 12-month [T3]
Other Adverse event Number of hypoglycaemia and extreme negative emotions as recorded in participant's diary 6-week (immediate post-intervention) [T1]
Other Adverse event Number of hypoglycaemia and extreme negative emotions as recorded in participant's diary 6-month [T2]
Other Adverse event Number of hypoglycaemia and extreme negative emotions as recorded in participant's diary 12-month [T3]
Primary Diabetes-related distress Measured with the 17-item Diabetes Distress Scale (DDS-17) 6-week (immediate post-intervention) [T1]
Primary Diabetes-related distress Measured with the 17-item Diabetes Distress Scale (DDS-17) 6-month [T2]
Primary Diabetes-related distress Measured with the 17-item Diabetes Distress Scale (DDS-17) 12-month [T3]
Secondary Depression Measured with the Patient Health Questionnaire (PHQ-9) 6-week (immediate post-intervention) [T1]
Secondary Depression Measured with the Patient Health Questionnaire (PHQ-9) 6-month [T2]
Secondary Depression Measured with the Patient Health Questionnaire (PHQ-9) 12-month [T3]
Secondary Illness perception Measured with the Brief Illness Perception Questionnaire (BIPQ) 6-week (immediate post-intervention) [T1]
Secondary Illness perception Measured with the Brief Illness Perception Questionnaire (BIPQ) 6-month [T2]
Secondary Illness perception Measured with the Brief Illness Perception Questionnaire (BIPQ) 12-month [T3]
Secondary Quality of life Measured with the WHOQOL-BREF 6-month [T2]
Secondary Quality of life Measured with the WHOQOL-BREF 12-month [T3]
Secondary Self-efficacy Measured by the Diabetes Management Self Efficacy Scale (DMSES) 6-week (immediate post-intervention) [T1]
Secondary Self-efficacy Measured by the Diabetes Management Self Efficacy Scale (DMSES) 6-month [T2]
Secondary Self-efficacy Measured by the Diabetes Management Self Efficacy Scale (DMSES) 12-month [T3]
Secondary Self-care behaviours Measured with the Diabetes Self-Care Activities (SDSCA) scale 6-week (immediate post-intervention) [T1]
Secondary Self-care behaviours Measured with the Diabetes Self-Care Activities (SDSCA) scale 6-month [T2]
Secondary Self-care behaviours Measured with the Diabetes Self-Care Activities (SDSCA) scale 12-month [T3]
Secondary Positive emotions Measure by the Positive Affects subscale of the Center for Epidemiologic Studies Depression Scale (PA-CESD) 6-week (immediate post-intervention) [T1]
Secondary Positive emotions Measure by the Positive Affects subscale of the Center for Epidemiologic Studies Depression Scale (PA-CESD) 6-month [T2]
Secondary Positive emotions Measure by the Positive Affects subscale of the Center for Epidemiologic Studies Depression Scale (PA-CESD) 12-month [T3]
Secondary HbA1c 6-week (immediate post-intervention) [T1]
Secondary HbA1c 6-month [T2]
Secondary HbA1c 12-month [T3]
Secondary Blood pressure systolic and diastolic blood pressure 6-week (immediate post-intervention) [T1]
Secondary Blood Pressure systolic and diastolic blood pressure 6-month [T2]
Secondary Blood pressure systolic and diastolic blood pressure 12-month [T3]
Secondary LDL-cholesterol lipid profiles 6-week (immediate post-intervention) [T1]
Secondary LDL-cholesterol lipid profiles 6-month [T2]
Secondary LDL-cholesterol lipid profiles 12-month [T3]
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