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Stress Coping Training for Nurses and Diabetes Control (SCT/T2MD/GLYCO)

8 de noviembre de 2026 actualizado por: MSAlshammari, The New Model of Care, Hail Health Cluster

Effectiveness of Psychological Stress and Coping Mechanism Training Program for Nurses and Its Impact on Glycemic Control Among Patients With Type 2 Diabetes Mellitus at the Hail Region

General Objectives

  1. To measure the effectiveness of the stress and coping mechanism training program that is meant to help nurses deal with occupational stress and at the same time provide healthcare services to Type 2 Diabetes Mellitus patients in the Hail Region.
  2. To find out the impact of increased ability of nurses to cope with stress and its consequences on blood glucose levels and health of patients with Type 2 Diabetes Mellitus.
  3. To explore the connection between nurses' psychological state and quality of the care offered to diabetic patients in the region.
  4. To examine the long-term effects of stress management techniques on the performance, emotional state, and engagement of nurses.
  5. To explore how training in stress and coping mechanisms could affect the establishment of an empathic environment that would make the patients adhere to diabetes management programs.
  6. To provide inputs into the elaboration of integrated healthcare programs that would take into consideration both psychological resilience of nurses and physiological stability of patients with diabetes and other chronic diseases.

Specific Objectives

  1. To measure occupational stress experienced by the nurses before and after attending a training course on psychological stress and coping methods.
  2. To determine the impact of the nurses' training program on patients' glucose control by measuring HbA1c.
  3. To determine the relationship between the coping methods used by the nurses and adherence of patients to medications, diet and other self-management practices.
  4. To find out the main coping methods used by the nurses which help to reduce stress and promote positive mood while providing nursing care to diabetic patients.
  5. To learn patients' perception of the quality of care and communication after attending the nurses' training program on psychological stress and coping mechanisms.
  6. To make recommendations about implementing the psychological training and stress management programs into the continuing professional education of nurses working in diabetes care units in Hail Region.

Research Questions

  1. What is the efficiency of the program aimed at the development of coping and stress training of nurses working with Type 2 Diabetes Mellitus patients in the Hail Region?
  2. Is there any effect of improved stress management skills of nurses on the level of glycemic control of their patients, which is measured in terms of HbA1c values?
  3. What are the connections between coping mechanisms of nurses and the adherence of their patients to prescribed treatment regimes?
  4. What kind of coping strategies help nurses to feel better psychologically and be more satisfied with their job while working with Type 2 Diabetes Mellitus patients?
  5. How does the implementation of stress and coping mechanisms training affect patients' perception of the quality of the care provided and communication with nurses?
  6. Can psychological training programs have an impact on health care delivery and patient outcomes among Type 2 Diabetes Mellitus patients in the Hail Region?

Descripción general del estudio

Descripción detallada

Type 2 Diabetes Mellitus (T2DM) is a chronic metabolic disorder characterized by insulin resistance and persistent hyperglycemia, which can lead to severe complications if not effectively managed. Nurses play a crucial role in patient education, self-management support, and promoting adherence to treatment plans; however, psychological stress and inadequate coping mechanisms among nurses can negatively impact the quality of care and patient outcomes. This study aimed to evaluate the effectiveness of a psychological stress and coping mechanism training program for nurses and its impact on glycemic control among patients with T2DM in the Hail Region, Saudi Arabia. A quasi-experimental design was utilized, involving nurses who participated in a structured training program focusing on emotional regulation, stress management, and coping strategies, while patients under their care were monitored for glycemic control using HbA1c and fasting blood glucose levels before and after the intervention. Findings demonstrated that nurses who completed the training program exhibited improved stress management, coping abilities, and patient communication skills, which corresponded with significant improvements in patient glycemic outcomes, including better HbA1c levels and adherence to self-management practices. The study concludes that implementing psychological stress and coping mechanism training for nurses has a positive and substantial effect on both nurse well-being and patient glycemic control, highlighting the importance of integrating such programs into nursing practice to enhance patient-centered care and chronic disease management in the Hail Region.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

204

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Ha'il Region
      • Ha'il, Ha'il Region, Arabia Saudita, 53224
        • Hail Health Cluster
        • Contacto:
          • Saad Abdullah Alrasheed, Doctorate
          • Número de teléfono: +966 55 3217877
          • Correo electrónico: IRB-HAIL@MOH.GOV.SA

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Registered nurses hold active registration, will be directly involved in the care of patients with T2DM, were willing to attend all training sessions, and will be available for follow-up assessments.
  • Patients will be adults with a confirm diagnosis of T2DM who will be followed up by a participating nurse and who provide informed consent.

Exclusion Criteria:

  • Nurses on long-term leave, those not involved in direct patient care, and those who had previously completed a comparable stress-management program.
  • Patients with comorbidities known to substantially affect glycemic control, or who were unable to complete the assessments.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Investigación de servicios de salud
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Experimental: Stress and Coping Training

Nurses will receive the 16-hour Psychological Stress and Coping Mechanism Training Program in four 4-hour sessions plus monthly follow-up, training manual and coping journals.

The intervention will be grounded in the Transactional Model of Stress and Coping (Lazarus and Folkman, 1984) and in Self-Efficacy Theory (Bandura, 1977). It will comprise 16 hours of face-to-face training delivered in four 4-hour sessions by the principal investigator, a registered nurse educator with training in stress management, to groups of nurses at the participating facilities.

Module 1 will address the nature of psychological stress in nursing, common stressors in diabetes care, and early signs of burnout. Module 2 will cover problem-focused and emotion-focused coping and will introduce mindfulness, relaxation, cognitive restructuring, and time-management techniques. Module 3 will examine how nurse stress may affect patient communication, adherence, self-management, and glycemic control, using case studies of nurse-patient interactions. Module 4 will focus on practical skills through role-play, simulated clinical scenarios, group problem-solving, and the use of stress logs and

Sin intervención: No Intervention: Usual Care

Nurses will continue routine nursing care for patients with Type 2 Diabetes Mellitus without the training program. Patients will receive standard diabetes care and follow-up.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Baseline Demographic and Professional Characteristics of Participating Nurses
Periodo de tiempo: Baseline, pre-intervention [Day 0, first face-to-face interview]

Demographic and professional characteristics collected using a researcher-designed form, including: gender, age group, marital status, educational level in nursing, years of nursing experience, job position, and nationality.

Baseline, pre-intervention [Day 0, first face-to-face interview]

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Perceived stress
Periodo de tiempo: Pretest, immediate post-test, and follow-up three months

Nurses' stress will be measure with the 14-item Perceived Stress Scale (PSS- 14; Cohen et al., 1983). Items are rated from 0 (never) to 4 (very often) with reference to the past month. The seven positively worded items (perceived self-efficacy/control) will be reverse score, and all items will be sum to give a total score from 0 to 56, with higher scores indicating greater stress. Subscale scores were computed for helplessness (seven negatively worded items, 0-28) and perceived self-efficacy/control (seven positively worded items, raw scoring, 0-28; higher scores indicating greater perceived control).

Pretest, immediate post-test, and follow-up three months
Coping strategies
Periodo de tiempo: Pretest, immediate post-test, and follow-up three months

Coping will be measure with the 29-item revised Ways of Coping Checklist (WCCL; Vitaliano et al., 1985), which comprises five subscales: problem-focused coping (12 items), seeking social support (3 items), self-blame (3 items), wishful thinking (6 items), and avoidance (5 items). Items are rated from 1 (not at all) to 4 (to a great extent).

Pretest, immediate post-test, and follow-up three months
Diabetes self-management self-efficacy
Periodo de tiempo: Pretest, immediate post-test, and follow-up three months

Patients will be complete the 20-item Diabetes Management Self-Efficacy Scale (DMSES; van der Bijl et al., 1999), which covers blood glucose monitoring (3 items), dietary control (10 items), physical activity (3 items), foot care (1 item), and medication intake and follow-up (3 items). Items are rated from 0 (cannot do at all) to 10 (certainly can do); total scores range from 0 to 200, with higher scores indicating greater self-efficacy, and were classified as low (<120), moderate (120-149), or high (≥150).

Pretest, immediate post-test, and follow-up three months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

15 de diciembre de 2026

Finalización primaria (Estimado)

15 de diciembre de 2026

Finalización del estudio (Estimado)

15 de abril de 2027

Fechas de registro del estudio

Enviado por primera vez

22 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

8 de noviembre de 2026

Publicado por primera vez (Actual)

12 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

8 de noviembre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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