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Active, Not Recruiting

NCT Number: NCT07025109

Assessing Peer Support for Physical Activity in Women With HIV and Hypertension

This clinical trial will assess the acceptability and feasibility of a peer-supported behavioral physical activity intervention for women living with HIV and Hypertension.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

40 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Department of Family & Community Medicine; University of Alabama at Birmingham

Birmingham, Alabama, 35205, United States

About this study

An individually randomized pilot trial (N=50) of an adapted behavioral physical activity (PA) intervention will be used to assess the feasibility and acceptability of providing exercise prescription, peer support, and home blood pressure monitoring to women ages 40+ living with HIV and Hypertension. Secondary outcomes to be assessed include systolic and diastolic blood pressure, PA time and intensity, PA self-efficacy, perceived social support, and health-related quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • woman living with HIV
  • age 40 and above
  • diagnosed with HTN
  • access to a personal phone for study-related phone calls
  • willing to wear an accelerometer on their waist or hip for 7 days at beginning and end of 12-week intervention
  • able to ambulate independently
  • English speaking

Exclusion criteria

  • Pregnant
  • unable to provide informed consent due to cognitive deficit, serious mental illness, or active substance use

Treatment and study plan

Peer Support

Behavioral

Peer support counseling will include phone or text communication to assess goal progress, provide motivational counseling as needed, and to provide social support.

Exercise Prescription

Behavioral

Women will be provided with an exercise prescription (Frequency, Intensity, Time, Type) which may be adjusted weekly for 6 weeks to goal of 150min/week of moderate to vigorous physical activity.

Blood pressure self monitoring

Behavioral

Women will receive a home blood pressure monitor and encourage to record their readings in a log.

Primary outcomes

  1. Participant attrition

    Time frame: From enrollment to end of 12 week intervention

    Measure of participants who withdraw from the behavioral trial in the intervention and the control groups to determine feasibility of enrolling and retaining individuals in the trial. Approximately 15% attrition is expected in a behavioral clinical trial. Higher levels of attrition relate to lower feasibility.

  2. Intervention acceptability: Satisfaction

    Time frame: Mid-point (6-week) assessment and end of intervention assessment (12-week)

    Participant satisfaction with the intervention: Treatment Satisfaction Questionnaire adapted for behavioral treatment. The measure includes 11 items asked on a Likert-type scale from 1=Extremely Dissatisfied to 7=Extremely Satisfied, with 3 items asked on a 1-5 scale. 1 item will be removed that asks about medication side effects. Scores can range from 10 to 64. Higher scores mean higher satisfaction with the treatment/intervention.

  3. Intervention Acceptability: Treatment burden

    Time frame: At 6-week (mid-point intervention) and 12-weeks (end of intervention)

    The Brief Patient Experiences with Treatment and Self Management will be used. The scale includes 32 items total. Most items use a 5-point Likert-type scale from 1=very easy to 5=very difficult. Some items use a 5-point Likert scale (agreement). And some use a Likert-type frequency/intensity measure from 1=not at all to 5=very much. Does not apply=0. Total scores range from 0 to 150. Higher scores mean higher treatment burden.

Secondary outcomes

  1. Systolic and diastolic blood pressure

    Time frame: Measured at baseline, 6-weeks (mid-point) and 12-weeks (end of intervention)

    Home blood pressure readings taken x3 and averaged.

  2. Daily physical activity: Accelerometer measured

    Time frame: Collected at baseline pre-randomization, and at 12-weeks (end of intervention)

    7-day accelerometer observation of daily physical activity

  3. Self reported physical activity

    Time frame: Collected at baseline, 6 weeks (mid-point), and 12-weeks (post-intervention)

    Time and intensity of physical activity via the International Physical Activity Questionnaire - Short Form (IPAQ-SF) which are then computed to a continuous score of MET (metabolic equivalents)-minutes per week. Computed as follows: Total PA METmin/week=[(3.3*walking minutes*walking days)+(4.0*moderate activity minutes*moderate activity days)+(8.0*vigorous activity minutes*vigorous activity days)]. Higher scores mean greater physical activity.

  4. Physical Activity Self Efficacy

    Time frame: Collected at baseline, 6-weeks (mid-point) and 12-weeks (post-intervention)

    Confidence to engage in regular physical activity will be measured using the Exercise Self Efficacy Scale. A total of 9 items are asked using a scale from 0=not at all confident to 10=completely confident. Scores range from 0-90. Higher scores mean higher self efficacy.

  5. Physical activity enjoyment

    Time frame: Collected at baseline, 6-weeks (mid-point), and 12-weeks (post-intervention)

    Physical activity enjoyment scale will be used. The scale has 18 items and each item is asked on a 1 to 7 scale. Scores may range from 18-126. Higher scores mean higher enjoyment and perceived positive outcomes from exercise/physical activity.

  6. Social support for physical activity

    Time frame: Collected at baseline, 6-weeks (mid-point), and 12-weeks (post-intervention)

    Social support for exercise behaviors scale will be used that includes 10 items asked on a scale from 1=none to 5=very often, there is also an option for does not apply. Scores range from 10-50. Higher scores mean more social support for physical activity.

Other outcomes

  1. General Social Support

    Time frame: Collected at baseline, 6-weeks (mid-point), and 12-weeks (post-intervention)

    Medical outcomes study social support scale will be used to assess global social support. The scale includes 19 items and the overall support index is calculated by taking the mean of all of the items resulting in a range from 1-5. Scores can be transformed to a 0-100 score by the following equation: 100*((observed score-minimum possible score)/(maximum possible score-minimum possible score)). Higher scores mean greater social support.

  2. Health related quality of life

    Time frame: Collected at baseline, 6-weeks (mid-point), and 12-weeks (post-intervention)

    The Short Form Health Survey-12 (SF-12) will be used to assess Health related quality of life (HRQoL) which asks about physical and emotional health in the past 4 weeks using 12 items. In scoring, all items are coded to yield a total score between 0 and 100 such that higher scores mean better HRQoL.

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Official study title

Adaptation and Pilot Testing a Behavioral Physical Activity Intervention With Peer Support for Women With HIV and Co-Occurring Hypertension

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 17, 2025
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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