- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04978974
Implications of Stress Management Program
July 24, 2021 updated by: Hafsa Qurban, University of Gujrat
Stress, Coping Strategies and Quality of Life Among Patients With Chronic Conditions: Implications of Stress Management Program
Previous studies indicated that patients with diabetes mellitus and hypertension had higher level of perceived stress, used maladaptive coping strategies and poor health-related quality of life.
Therefore, stress management program was applied to reduce their perceived stress, improve their coping strategies, improve their health-related quality of life and psychological health of the patients with type 2 diabetes mellitus and hypertension in current study.
The main objectives of the current study were to observe the effects of stress management program on perceived stress, coping strategies and health-related quality of life using pre-experimental research design.
Patients with diabetes mellitus type 2 and hypertension were selected through purposive sampling technique to apply the eclectic approach of the stress management program.
Total 110 patients with type 2 diabetes and hypertension completed the program from 114 patients who gave inform consent for participation in the first session.
Perceived stress scale, WHOQOL and Coping strategies questionnaire were administered at the pre and post-levels of the program.
Further, base line of targeted domains variables was also filled from the participants at pre, mid and post-levels to access the efficacy of the program which was formulated according to previous research data by the researcher.
The stress Management program consisted of 10 session which were delivered to eight groups (diabetic and Hypertensive) in five weeks.
Each session had the duration 90 minutes and two sessions were conducted in one week.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
110
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Punjab
-
Jhelum, Punjab, Pakistan
- Jhelum Poly Clinic
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
31 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients with type II diabetes or hypertension with at least three months duration of illness
- had not attended any psychological intervention or stress management program earlier
Exclusion Criteria:
- Patients who had any other physical/ mental illnesses along with diabetes or hypertension
- Patients with type I diabetes
- Patients with gestational diabetes or hypertension
- Had diabetes or hypertensive condition from less than three month
- Had co morbidity of diabetes and hypertensive chronic conditions
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Patients with type 2 Diabetes mellitus and Hypertension
patients with type 2 diabetes mellitus and hypertension were selected by using purposive sampling technique to apply stress management program
|
Stress management program includes different techniques such as relaxation technique, psycho-education, laughing, emotional freedom technique, referenting, cognitive restructuring, rational emotive imagery, time management, anger management, assertiveness and social support
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effects of stress management program as assessed using Perceived Stress Scale
Time Frame: 10th session (one month and one week from first assessment)
|
Consisted of 10 items, Scoring: 0 to 1, The Higher score shows more stress
|
10th session (one month and one week from first assessment)
|
|
Effects of stress management program as assessed using Health-Related Quality of Life
Time Frame: 10th session (one month and one week from first assessment)
|
Consisted of 26 items, Scoring: 1 to 5, The higher score shows better HRQOL
|
10th session (one month and one week from first assessment)
|
|
Effects of stress management program as assessed using Coping Strategies Questionnaire
Time Frame: 10th session (one month and one week from first assessment)
|
Consisted of 62 items, Scoring: 1 to 5, The higher score shows high use of coping strategies
|
10th session (one month and one week from first assessment)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effects of stress management program as assessed using Baseline
Time Frame: base line were used in 5th (two weeks and 3 days) and 10th session (one month and one week from first assessment)
|
20 targeted domains which included information about the illness, information about the causes of illness, information about the treatment of illness, efforts to control the level of illness, application of domestic tips, hopefulness, anxiety, negative thoughts, problems in daily activities, problems in social relationships, anger, appetite problems, sleep problems, concentration problems, body pain, fatigue, absent mind, unhealthy diet, loneliness and restlessness at pre, mid and post levels of stress management program.
Rating scale ranges from 0-10 (0 shows there is absence of the target construct while 10 shows the high level of target construct).
|
base line were used in 5th (two weeks and 3 days) and 10th session (one month and one week from first assessment)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 3, 2019
Primary Completion (Actual)
January 3, 2020
Study Completion (Actual)
December 29, 2020
Study Registration Dates
First Submitted
June 27, 2021
First Submitted That Met QC Criteria
July 24, 2021
First Posted (Actual)
July 27, 2021
Study Record Updates
Last Update Posted (Actual)
July 27, 2021
Last Update Submitted That Met QC Criteria
July 24, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UOG/ASRB/Psych/3/18631/011
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Due to data confidentiality from the participants, there is no plan of IPD available
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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