- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06064110
Pictou County PEP: A 6-Month, Home-Based, Personal Empowerment Program for Adults With a Chronic Medical Condition Living in Pictou County
December 17, 2025 updated by: Gabriela Ilie, Nova Scotia Health Authority
Pictou County PEP: A Phase 2 Trial of a Six-Month Home-Based Personal Empowerment Program to Improve the Mental and Physical Health of Adults With a Chronic Medical Condition Living in Pictou County
The Pictou County Personal Empowerment Program is a comprehensive health promotion program aiming to improve the quality of life as well as both physical and mental health in Adults living with chronic medical conditions.
The program includes daily email communications over 6 months that encourage a range of self-management and health promoting activities, including strength and aerobic exercise, yoga, stress reduction techniques, dietary improvements, relationship/intimacy education and more.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
185
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
-
-
Nova Scotia
-
Halifax, Nova Scotia, Canada
- QEII Health Sciences Centre
-
New Glasgow, Nova Scotia, Canada
- Aberdeen Hospital
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
INCLUSION CRITERIA:
- Age >18;
Diagnosed with one or more chronic medical conditions, as per the participant's report, including but not restricted to the following (complete list in protocol appendix):
- Heart disease / cardiovascular disease / stroke
- High blood pressure
- Diabetes including a diagnosis of pre-diabetes
- Chronic respiratory disease
- Chronic neurologic disease
- Chronic kidney disease
- Chronic liver disease
- Immunodeficiency
- Overweight or Obese (BMI >25)
- Psychiatric or mental health issue - e.g., depression and anxiety
- Substance-related and addictive disorders (e.g alcohol, smoking, etc.);
- Resident of Pictou County, Nova Scotia;
- Existing (or willingness to create) email account and willingness to access email daily;
- Ability to follow website links to watch YouTube videos;
- Ability to understand and speak English;
- Ability to participate in low to moderate levels of physical activity and strength training;
- Ability and willingness to fill out an online survey at baseline, and 6, 12 months, and fill in a weekly compliance survey for the six months of the program.
EXCLUSION CRITERIA:
- Diagnosed with cancer in the last 5 years and/or received treatment for cancer in the last 5 years;
- Myocardial infarction or stroke within the last year AND without written approval from their Family Physician, Cardiologist, or Study Physician that they are safe to exercise;
- Unable to access the internet daily during the intervention;
- Lack of access to a computer or smartphone to receive emails required for study intervention.
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: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention arm
|
The 6 month home-based program focuses on aerobic and strength training, meditation/relaxation techniques, social connection, and overall healthy lifestyle practices supported with daily email reminders.
The aerobic (5 times/week) and strength (2 times/week) program will comprise of a single 30-minute session daily, the meditation/relaxation practice is 10 minutes daily, the intimacy and connection component consists of engaging in at least one form of intimacy practice prescribed, per day.
Optional social connection components will be offered, such as pairing participants up with peers from the study, monthly Zoom videoconferences, and monthly in-person events in Pictou County to further promote healthy lifestyle habits.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mental Health as assessed by the Kessler Kessler Psychological Distress Scale (K10)
Time Frame: 6-12 months
|
A 10 item questionnaire that assesses psychological distress.
The scale has a score range of 10-50, with higher scores indicating worse mental health.
|
6-12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Personality as assessed by the Ten-Item Personality Inventory (TIPI)
Time Frame: 6-12 months
|
A 10 item questionnaire assessing the Big-Five personality dimensions (Extraversion, Agreeableness, Conscientiousness, Emotional Stability, Openness to Experiences).
The scale has a score range of 1-14 for each dimension with higher scores indicating a higher level of that personality trait.
|
6-12 months
|
|
Diet assessed by the Rapid Eating Assessment for Participants (REAP-S).
Time Frame: 6-12 months
|
A 16 item questionnaire assessing diet quality.
The scale has a score range of 13-39 with a higher score indicating a higher diet quality.
|
6-12 months
|
|
Sleep Quality as assessed by the Pittsburgh Sleep Quality Index (PSQI)
Time Frame: 6-18 months
|
A 19 item questionnaire that assesses sleep quality and disturbances.
The scale has a score range of 0-21 with a higher score indicating worse sleep quality.
|
6-18 months
|
|
Sedentary behaviour measured by the Sedentary Behaviour Questionnaire (SBQ) for Adults.
Time Frame: 6-12 months
|
Two 9 item questionnaires (weekday and weekend) with each item scored to none to 6 hours or more.
The total score is the sum of the amount of time and as it increases it indicates higher amount of sedentary behaviour.
|
6-12 months
|
|
Anxiety severity assessed by the GAD-7.
Time Frame: 6-12 months
|
A 7 item questionnaire with scores ranging from 0-21 higher scores indicating more severe level of anxiety.
|
6-12 months
|
|
Relationship satisfaction as assessed by the Dyadic Adjustment Scale (RDAS-14).
Time Frame: 6-12 months
|
A 14 item questionnaire that measure an individual's perceptions of their relationship with an intimate partner.
The scale has a total score range of 1-151 with a higher score indicating better satisfaction.
|
6-12 months
|
|
Center for Epidemiologic Studies Depression Scale (CES-D).
Time Frame: 6-12 months
|
A 20 item questionnaire with a possible range of scores from zero to 60, with the higher scores indicating the presence of more depressive symptomatology.
|
6-12 months
|
|
Satisfaction with Life Scale (SWLS).
Time Frame: 6-12 months
|
A 5 item questionnaire that was designed to measure subjective well-being.
Scores range from 5-35 with higher scores indicating higher satisfaction with life.
|
6-12 months
|
|
Incidence and severity of participant self-reported adverse events
Time Frame: 6-12 months
|
6-12 months
|
|
|
The Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F)
Time Frame: 6-12 months
|
A 40-item measure that assesses self-reported fatigue and its impact upon daily life, using a 5 point Likert-type scale with values ranging from 0-5, where higher scores represent worse outcomes.
|
6-12 months
|
|
Alcohol Habit assessed by questions from the National Health Institute Alcohol Consumption questionnaire.
Time Frame: 6-12 months
|
Questions assessing alcohol consumption using semantic differential scales that have a range of up to 11 response options.
Response options range from never consuming alcohol to daily consumption, as well as consuming no alcohol each day to 25+ drinks a day on average, with higher scores being worse.
|
6-12 months
|
|
Smoking habit assessed by the Global Adult Tobacco Survey 2020 (GATS).
Time Frame: 6-12 months
|
Questions assessing current and past smoking habit using semantic differential scales with possible answers ranging from daily smoking to not smoking at all.
Lower scores indicate higher smoking habit/worse outcome.
|
6-12 months
|
|
Comorbidity level assessed by the modified Charlson Comorbidity Index (CCI)
Time Frame: 6-12 months
|
A 21 item questionnaire that uses a weighted index to assess the quantity and severity of comorbidities a patient has.
Each comorbidity category has a related weight, ranging on a scale of 1-6, with higher scores representing worse outcomes.
|
6-12 months
|
|
Availability of social support assessed by the MOS Social Support Survey
Time Frame: 6-12 months
|
A 19 item questionnaire that assesses emotional/informational support, positive social interaction, tangible support and affectionate support.
Higher item scores reflect a higher level of social support.
|
6-12 months
|
|
Brief Illness Perception Questionnaire (BIPQ)
Time Frame: 6-12 months
|
A 9 item scale that measures an individual's beliefs, feelings, and cognitive representations of one's illness.
This questionnaire uses linear numeric scales with response options ranging from 0-10.
Total scores can range from 0-80, with higher scores representing worse illness perceptions.
|
6-12 months
|
|
Perceived Stress Scale (PSS-10)
Time Frame: 6-12 months
|
A 10-item scale that measures a person's perceived feelings of stress during the last month.
This questionnaire uses a Likert-type scale with response options scores ranging from 0-4.
Scores on the PSS-10 can range from 0-40 with higher scores indicating higher perceived stress.
|
6-12 months
|
|
WHO-5 Well-Being Index
Time Frame: 6-12 months
|
A short, 5-item, generic global rating scale measuring subjective well-being using a Likert-type scale.
Scores range from 0-5, with higher scores indicating better well-being.
|
6-12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
November 24, 2023
Primary Completion (Actual)
May 14, 2025
Study Completion (Actual)
October 28, 2025
Study Registration Dates
First Submitted
September 26, 2023
First Submitted That Met QC Criteria
September 26, 2023
First Posted (Actual)
October 3, 2023
Study Record Updates
Last Update Posted (Actual)
December 23, 2025
Last Update Submitted That Met QC Criteria
December 17, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pictou-County-PEP
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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